S. Roberts

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Introduction to Biocatalysis, Using Enzymes and Microorganisms.

M. Turner, N. Turner, S. Roberts, 1995 .

Introduction to Biocatalysis Using Enzymes and Micro-Organisms: Contents

M. Turner, N. Turner, S. Roberts, 1995 .

Medicinal Chemistry: The Role of Organic Chemistry in Drug Research

C. Ganellin, S. Roberts, 1985 .

Introduction to enzymes, receptors and the action of small molecule drugs

A. Gibb, S. Roberts, 2013 .

Enzymic polymerisation of an unactivated diol/diacid system

S. Roberts, F. Binns, Alan H. Taylor, 1993 .

Studies leading to the large scale synthesis of polyesters using enzymes

S. Roberts, F. Binns, Alan H. Taylor, 1999 .

Reactions of some cyclopentenones with selected cysteine derivatives and biological activities of the product thioethers.

A. Ciucci, M. Santoro, P. Evans, 2004, Bioorganic & medicinal chemistry.

Synthesis and revision of the stereochemistry of a cyclopentenone natural product isolated from ascomycete strain A23-98

T. Snape, M. Santoro, S. Roberts, 2004 .

Recent advances in the generation of chiral intermediates using enzymes.

R. H. Green, H. G. Davies, S. Roberts, 1990, Critical reviews in biotechnology.

The oxidation of norbornadiene and some derivatives using Pseudomonas sp.

G. Ryback, S. Roberts, R. J. Pryce, 1990 .

Preparation of carbocyclic, phosphonate analogues of cyclic adenosine monophosphate (cAMP)

S. Roberts, Jennifer M. L. Hillman, 1997 .

Biotransformation of endo-bicyclo[2.2.1 ]heptan-2-ols and endo-bicyclo[3.2.0]hept-2-en-6-ol into the corresponding lactones

C. Knowles, N. Shipston, S. Roberts, 1991 .

Biphasic one-pot synthesis of two useful and separable compounds using nicotinamide cofactor-requiring enzymes: Syntheses of (S)-4-hydroxyhexanoate and its lactone

Chi‐Huey Wong, S. Roberts, D. Drueckhammer, 1987 .

Enzymatic resolution of oxalate esters of a tertiary alcohol using porcine pancreatic lipase

N. Turner, S. Roberts, R. Mccague, 1993 .

Camphor-grown Pseudomonas putida, a multifunctional biocatalyst for undertaking Baeyer-Villiger monooxygenase-dependent biotransformations

G. Grogan, S. Roberts, A. Willetts, 1993, Biotechnology Letters.

Comparison of microbiologically and enzymatically mediated Baeyer–Villiger oxidations: synthesis of optically active caprolactones

V. Alphand, R. Furstoss, S. Roberts, 1996 .

Biological Baeyer–Villiger oxidation of some monocyclic and bicyclic ketones using monooxygenases from Acinetobacter calcoaceticus NCIMB 9871 and Pseudomonas putida NCIMB 10007

G. Grogan, R. Gagnon, S. Roberts, 1994 .

Microbial oxidation of 7endo-methylbicyclo[3.2.0]hept-2-en-6-one, 7,7-dimethylbicyclo[3.2.0]hept-2-en-6-one and 2exo-bromo-3endo-hydroxy-7,7-dimethylbicyclo[3.2.0]heptan-6-one using Acinetobacter NCIMB 9871

V. Šik, S. Roberts, A. Willetts, 1991 .

Enzyme-catalysed baeyer–villiger oxidations of some substituted bicyclo[3.2.0]heptanones

V. Šik, S. Roberts, A. Willetts, 1990 .

Biotransformations Relating to Heterocyclic Compounds

S. Roberts, 1989 .

Highly diastereoselective inter-esterification reactions involving a racemic acetate and a racemic carboxylic acid catalysed by lipase enzymes

P. Fowler, S. Roberts, E. Macfarlane, 1991 .

Catalysts for Fine Chemical Synthesis

S. Roberts, G. Poignant, 2002 .

The emergence of the cyclopentenone prostaglandins as important, biologically active compounds

M. Santoro, S. Roberts, Eugene S. Sickle, 2002 .

Synthesis of a potent inhibitor of HIV reverse transcriptase

C. Hamilton, S. Roberts, A. V. Shipitsin, 1998 .

Enzyme-catalysed inter-esterification procedure for the preparation of esters of a chiral secondary alcohol in high enantiomeric purity

N. Turner, S. Roberts, E. Macfarlane, 1990 .

Enzyme-catalysed esterification of (±)-trans-cyclohexane-1,2-dimethanol

S. Roberts, P. Taylor, V. G. R. Steukers, 1993 .

Some Interesterification Reactions Involving Mucor Miehei Lipase

N. Turner, S. Roberts, F. Rebolledo, 1991 .

Adenosine A1 and A3 selective N‐alkoxypurines as novel cytokine modulators and neuroprotectants

C. Thomsen, M. Sheardown, S. Roberts, 1998 .

Synthesis of compounds active against HIV. Part 2. Preparation of some 2′,3′-dideoxy-6′-fluorocarbocyclic nucleosides

D. Coe, S. Roberts, D. Parry, 1990 .

Synthesis, antimalarial activity, biomimetic iron(II) chemistry, and in vivo metabolism of novel, potent C-10-phenoxy derivatives of dihydroartemisinin.

B. K. Park, S. Ward, P. O’Neill, 2001, Journal of medicinal chemistry.

Synthesis of optically active allenes using tandem enzyme and palladium-catalysed reactions

S. Roberts, P. Dixneuf, T. Guyot, 1997 .

Biotransformations by microbial Baeyer-Villiger monooxygenases stereoselective lactone formationin vitro by coupled enzyme systems

G. Grogan, S. Roberts, A. Willetts, 1992, Biotechnology Letters.

Biotransformation of cycloalkanediones by microorganisms; Stereoselective reduction of (±)-camphorquinone

S. Roberts, A. Willetts, F. Rebolledo, 1991, Biotechnology Letters.

Use of Enzymes as Catalysts in Key Reactions Leading to the Synthesis of Optically Active Natural Products and Analogues

N. Turner, S. Roberts, 1992 .

7 – Recent Developments in the Use of Enzyme-Catalysed Reactions in Organic Synthesis

S. Roberts, 1990 .

Use of enzymes as catalysts to promote key transformations in organic synthesis

S. Roberts, 1989 .

Enzymes as Catalysts in Organic Synthesis

S. Roberts, 1989 .

Substrate non-enantiospecific and product enantioselective reduction of bicyclo[3.2.0]hept-2-en-6-one using yeast

D. Reynolds, R. Newton, S. Roberts, 1979 .

Enzymes in Organic Synthesis

S. Roberts, 1990 .

Enzymatic kinetic resolution of 1,1-dioxo-2,3-dihydro-1H-1λ6-thiophen-3-ol via temporary derivatisation

P. Evans, S. Roberts, B. Morgan, 2006 .

A synthetic approach to squalestatin 1

Joseph P. Adams, H. Abdel-Rahman, D. Slee, 1993 .

New modified nucleoside 5′-triphosphates: synthesis, properties towards DNA polymerases, stability in blood serum and antiviral activity

R. Beabealashvilli, A. Krayevsky, C. Hamilton, 1999 .

Synthesis of some mimics of nucleoside triphosphates

M. Peel, D. Coe, R. Storer, 1991 .

Design of Anti-Viral Agents Other than Nucleoside Analogues

S. Roberts, 1988 .

Synthesis and biological activity of the novel nitric oxide synthase inhibitor Nω′-hydroxy-Nω-methyl-L-arginine

T. Warner, E. Änggård, H. Moynihan, 1994 .

Model for the functional active site of Baeyer–Villigerases. X-Ray crystal data for (1S,2R,5R,8S,1′R)-8-endo-benzoyloxy-N-(1′-phenylethyl)bicyclo[3.3.0]octane-2-endo-carboxamide

D. Hibbs, C. Knowles, M. A. Wright, 1995 .

Enzymatic Baeyer–Villiger oxidations of some bicyclo[2.2.1]heptan-2-ones using monooxygenases from Pseudomonas putida NCIMB 10007: enantioselective preparation of a precursor of azadirachtin

R. Villa, G. Grogan, R. Gagnon, 1995 .

Development of the enzyme-catalysed Baeyer–Villiger reaction as a useful technique in organic synthesis

S. Roberts, A. Willetts, 1993 .

Stereoselective alkene synthesis via silicon-directed [2,3]-sigmatropic rearrangements: an approach to leukotrienes

S. Roberts, G. Pattenden, John E. Crawley, 1993 .

Use of the two enantiometers of 7,7-dimethylbicyclo[3.2.0]hept-2-en-6-one to form complementary optically active synthons in a convergent synthesis of leukotriene-B4

G. Dormán, S. Roberts, B. Wakefield, 1991 .

Synthesis of (+)-brefeldin-A

S. Roberts, A. Willetts, H. Olivo, 1994 .

Synthesis of fluorinated phosphonoacetate derivatives of carbocyclic nucleoside monophosphonates and activity as inhibitors of HIV reverse transcriptase

C. Hamilton, S. Roberts, 1999 .

PREPARATION OF POLYAMINO ACID CATALYSTS FOR USE IN JULIA ASYMMETRIC EPOXIDATION

J. Littlechild, W. Kroutil, S. Roberts, 1997 .

Chemoenzymatic, enantiocomplementary, total asymmetric synthesis of leukotrienes-B3 and -B4

G. Dormán, K. Faber, S. Roberts, 1990 .

The application of microbial methods to the synthesis of chiral fine chemicals

N. Turner, S. Roberts, 1997 .

Carbocyclic adenosine phosphates as nucleotide mimics in some enzyme-catalysed reactions

S. Roberts, D. Grand, 1993 .

Probing the effect of a 3'-S-phosphorothiolate link on the conformation of a DNA:RNA hybrid; implications for antisense drug design.

J. Arnold, J. Fisher, S. Roberts, 2002, Chemical communications.

2-Substituted-2,4-endo-dimethyl-8-oxabicyclo[3.2.1]octan-3-ones as catalysts for the asymmetric epoxidation of some alkenes with Oxone®

S. Roberts, S. Klein, 2002 .

Reduction of bicyclo[3.2.0] hept-2-en-6-one and 7,7-dimethylbicyclo[3.2.0]hept-2-en-6-one using dehydrogenase enzymes and the fungus mortierella ramanniana

W. F. Wall, M. Turner, M. Dawson, 1985 .

The potential of carbocyclic nucleosides for the treatment of AIDS: synthesis of carbocyclic 6′-fluoro-2′,3′-dideoxythymidine

D. Coe, R. Storer, S. Roberts, 1991 .

Preparation of nucleotide mimics with potent inhibitory activity against HIV reverse transcriptase

D. Coe, R. Storer, S. Roberts, 1991 .

Synthesis and biological activity of lactones en route to Altohyrtin A.

S. Roberts, A. Murphy, S. Hermitage, 1998, Bioorganic & medicinal chemistry letters.

Oxidative biotransformations by microorganisms: Stereoselective sulfoxide formation by Saccharomyces cerevisiae

P. Richardson, S. Roberts, A. Willetts, 1995, Biotechnology Letters.

Polyhalogeno-aromatic compounds. Part XVI. The preparation and reactions of polyhalogenophenyl- and polyhalogenopyridyl-hydrazines

I. Collins, S. Roberts, H. Suschitzky, 1971 .

Improved procedure for Juliá–Colonna asymmetric epoxidation of α,β-unsaturated ketones: total synthesis of diltiazem and TaxolTM side-chain

S. Roberts, R. Mccague, T. Nugent, 1997 .

Site selective oxidation of tricyclo[3.3.1.13,7]decane (adamantane) and some of its derivatives using fungi of the genus Absidia

C. Ridyard, G. Rosair, P. Bailey, 1996 .

REACTION OF CERIUM(IV) AMMONIUM NITRATE WITH 3‐METHYLCEPHALOSPORINS: SYNTHESIS OF A 2‐METHOXY‐3‐METHYLCEPHALOSPORIN

Jon L. Wright, S. Roberts, R. Fletton, 1985 .

Conversion of Some Cephalosporins Into the 2-Alkoxy Derivatives Using Alkanolic Ceric (IV) Ammonium Nitrate

S. Roberts, D. C. Humber, 1985 .

Synthesis of a novel fluoro-tribactam utilising an N-fluorosulfonimide in the key step

Alessandro Padova, S. Roberts, D. Donati, 1996 .

Synthesis of a novel fluoro-tribactam utilising N-fluorosulfommide in the key step

Alessandro Padova, S. Roberts, D. Donati, 1995 .

Some Reactions of α-Trifluoromethylsulphonyloxy-Penicillanate Esters

S. Roberts, P. Mooney, J. Kemp, 1982 .

Unexpected configurational and conformational preference in bicyclo[3.2.0]heptane systems

S. Roberts, S. Toppet, A. Dreiding, 1982 .

Polymer-supported monodentate phosphite ligands for asymmetric hydrogenation

S. Roberts, Weiping Chen, J. Whittall, 2006 .

Polychloroaromatic compounds. Part I. Oxidation of pentachloropyridine and its NN-disubstituted amino-derivatives with peroxyacids

S. Roberts, H. Suschitzky, 1968 .

Microbial Transformation of (+)-10β,14-Dihydroxy-allo-aromadendrane and (–)-allo-Aromadendrone

S. Roberts, A. Carnell, Dênis P. Lima, 1999 .

Preparative biotransformations: the employment of enzymes and whole-cells in synthetic organic chemistry

S. Roberts, 1998 .

Bakers' yeast oxidation of methyl para-tolylsuifide: Synthesis of a chiral intermediate in the preparation of the mevinic acid-type hypocholestemic agents

S. Roberts, A. Willetts, J. Beecher, 1995 .

Biooxidations of some N-arylpiperidines and related compounds using Beauveria sulfurescens

S. Roberts, A. Willetts, N. Floyd, 1993 .

Microbial hydroxylation of cyclohexylcyclohexane:Synthesis of an analogue of leukotriene-B3

W. F. Wall, M. Turner, M. Dawson, 1986 .

Site selective oxidation of some azaspiroundecanes using Beauvaria sulfurescens ATCC 7159

S. Roberts, A. Willetts, W. Carruthers, 1990 .

Biotransformation of cycloalkenones; Controlled oxidative and reductive bioconversions byPseudomonas putida

G. Grogan, S. Roberts, A. Willetts, 1994, Biotechnology Letters.

Enzymatic esterification and de-esterification of carbohydrates: synthesis of a naturally occurring rhamnopyranoside of p-hydroxybenzaldehyde and a systematic investigation of lipase-catalysed acylation of selected arylpyranosides

S. Phythian, A. Reason, S. Roberts, 1995 .

Preparation of some novel S-nitroso compounds as potential slow-release agents of nitric oxide in vivo

H. Moynihan, S. Roberts, 1994 .

Synthesis of esters of the potent anti-bacterial trinems and analogues

S. Roberts, D. Donati, T. Rossi, 1996 .

Chemistry of 2-azabicyclo[2.2.1 ]heptan-3-one derivatives: role of the nitrogen atom in determining the stereochemistry of products isolated after formation of an incipient carbocation at C-6

V. Šik, S. Roberts, K. Parry, 1991 .

Syntheses of novel biologically active organofluorine compounds

S. Roberts, 1989 .

JULIA-COLONNA ASYMMETRIC EPOXIDATION REACTIONS UNDER NON-AQUEOUS CONDITIONS : RAPID, HIGHLY REGIO- AND STEREO-SELECTIVE TRANSFORMATIONS USING A CHEAP, RECYCLABLE CATALYST

S. Roberts, Joanne V. Allen, N. Williamson, 1998 .

Asymmetric epoxidation of enones employing polymeric α-aminoacids in non-aqueous media

D. Hibbs, M. Hursthouse, S. Roberts, 1997 .

Conversion of benzene and chlorobenzene into polyhydroxylated cyclohexane derivatives related to cyclophellitol

S. Roberts, P. W. Sutton, 1995 .

Resolution of 7,7-dimethylbicyclo[3.2.0]hept-2-en-6-one using Mortierella ramanniana and 3α,20β-hydroxy-steroid dehydrogenase, photochemistry of 3-hydroxy-7,7-dimethylbicyclo[3.2.0]heptan-6-ones, and the synthesis of (+)-eldanolide

W. F. Wall, M. Turner, M. Dawson, 1987 .

The use of enzymes for the catalysis of key reactions in the synthesis of biologically active natural products and analogues

S. Roberts, 1992 .

Whole cell catalysed kinetic resolution of 6-azabicyclo[3.2.0]hept-3-en-7-one: synthesis of (–)-cispentacin (FR 109615)

C. Evans, S. Roberts, A. Sutherland, 1991 .

Enantioselective synthesis of the hydroxy-lactone moiety of mevinic acids

S. Roberts, H. Olivo, R. Mccague, 1993 .

The isomerisation of (Z)-3-[2H1]-phenylprop-2-enone as a measure of the rate of hydroperoxide addition in Weitz-Scheffer and Julia-Colonna epoxidations.

S. Roberts, W. Heal, D. Kelly, 2004, Chemical communications.

Some regioselective cross-coupling reactions of halopyridines and halopyrimidines

A. Baxter, S. Roberts, D. Parry, 2002 .

Oligopeptides as catalysts for asymmetric epoxidation.

S. Roberts, D. Kelly, 2006, Biopolymers.

Polyamino acids as synthetic enzymes: mechanism, applications and relevance to prebiotic catalysis.

S. Colonna, A. Lazcano, G. Carrea, 2005, Trends in biotechnology.

The mechanism of polyleucine catalysed asymmetric epoxidation.

S. Roberts, D. Kelly, 2004, Chemical communications.

Development of the Juliá−Colonna Asymmetric Epoxidation Reaction: Part 1. Preparation and Activation of the Polyleucine Catalyst

J. Skidmore, J. Sander, S. Roberts, 2003 .

Efficient Asymmetric Epoxidation of α,β-Unsaturated Ketones Using a Soluble Triblock Polyethylene Glycol−Polyamino Acid Catalyst

J. Skidmore, M. Volk, S. Roberts, 2001 .

Polyamino acids as catalysts in asymmetric synthesis.

J. Skidmore, S. Roberts, M. Porter, 1999, Bioorganic & medicinal chemistry.

Polyamino acid-catalysed asymmetric epoxidation: Sodium percarbonate as a source of base and oxidant

J. Skidmore, S. Roberts, Joanne V. Allen, 1999 .

A new procedure for the Juliá–Colonna stereoselective epoxidation reaction under non-aqueous conditions: the development of a catalyst comprising polyamino acid on silica (PaaSiCat)

S. Roberts, T. Geller, 1999 .

Towards a mechanistic insight into the Juliá-Colonna asymmetric epoxidation of α,β-unsaturated ketones using discrete lengths of poly-leucine

S. Roberts, P. A. Bentley, M. Cappi, 1998 .

New procedures for the Juliá–Colonna asymmetric epoxidation: synthesis of (+)-clausenamide

J. Skidmore, S. Roberts, Yongxiang Liao, 1998 .

DEVELOPMENT OF THE JULIA ASYMMETRIC EPOXIDATION REACTION. PART 2. APPLICATION OF THE OXIDATION TO ALKYL ENONES, ENEDIONES AND UNSATURATED KETO ESTERS

P. Mayon, W. Kroutil, S. Roberts, 1996 .

Asymmetric hydrogenation reactions mediated by a new class of bicyclic bisphosphinites

M. Burk, S. Roberts, N. Derrien, 1999 .

PaaSicats: Powerful catalysts for asymmetric epoxidation of enones. Novel syntheses of α-arylpropanoic acids including (S)-fenoprofen

H. Davies, S. Roberts, Lydia Carde, 1999 .

SYNTHESIS OF OPTICALLY ACTIVE 2,3-SUBSTITUTED-1,2,3,4-TETRAHYDRO-4-QUINOLONES USING POLYLEUCINE

M. Hursthouse, S. Roberts, K. Malik, 1998 .

Ferrocene-based aminophosphine ligands in the Ru(II)-catalysed asymmetric hydrogenation of ketones : assessment of the relative importance of planar versus carbon-centred chirality

S. Roberts, Weiping Chen, J. Whittall, 2006 .

Regioselective acylation of carbohydrate derivatives using lipases leading to a facile two-step procedure for the separation of some α- and β-glucopyranosides and galactopyranosides

S. Roberts, P. Wan, P. Gonçalves, 2004 .

Juliá–Colonna stereoselective epoxidation of some α,β-unsaturated enones possessing a stereogenic centre at the γ-position: synthesis of a protected galactonic acid derivative

S. Roberts, P. Ray, 2001 .

Stereoselective synthesis of ferrocene-based C2-symmetric diphosphine ligands: application to the highly enantioselective hydrogenation of alpha-substituted cinnamic acids.

S. Roberts, Weiping Chen, P. Mccormack, 2007, Angewandte Chemie.

A very simple, highly stereoselective and modular synthesis of ferrocene-based P-chiral phosphine ligands.

S. Roberts, Weiping Chen, J. Whittall, 2006, Journal of the American Chemical Society.

Carbon–carbon bond formation at the C-4 position of an azetidin-2-one ring by intermolecular radical coupling reactions: a route to tribactams

Alessandro Padova, S. Roberts, D. Donati, 1994 .

An excellent reagent for the removal of the t-butyldimethylsilyl protecting group

D. Reynolds, R. Newton, S. Roberts, 1979 .

Preparation of carbocyclic analogues of 2′-deoxyribonucleotides possessing a phosphonate substituent at the 5′-position

A. Drake, A. Garofalo, S. Roberts, 1996 .

Efficient procedures for the large-scale preparation of (1S,2S)-trans-2-methoxycyclohexanol, a key chiral intermediate in the synthesis of tricyclic β-lactam antibiotics

M. Dawson, G. Webb, D. Noble, 1996 .

Synthesis of Esters of the Potent Antibacterial Trinems and Analogues.

S. Roberts, D. Donati, T. Rossi, 1997 .

Poly-L-leucine catalysed epoxidation reactions: A short, stereoselective route to chiral α,β-epoxyalcohols

M. Hursthouse, S. Roberts, K. Malik, 1998 .

Preparation of some novel prostanoids based on a tetrahydropyran ring system

M. Kelly, S. Roberts, 1991 .

Comprar Catalysts for Fine Chemical Synthesis, Volume 5, Regio- and Stereo-Controlled Oxidations and Reductions | Klaus D. Elgert | 9780470090220 | Wiley

S. Roberts, K. D. Elgert, J. Whittall, 2007 .

Mechanistic insights from reaction progress kinetic analysis of the polypeptide-catalyzed epoxidation of chalcone.

D. Blackmond, Suthahari Gunathilagan, S. Roberts, 2005, Organic letters.

Preparation of optically active 6′-fluorocarbocyclic nucleosides utilising an enantiospecific enzyme-catalysed Baeyer–Villiger type oxidation

R. Newton, S. Roberts, A. Willetts, 1990 .

Oxidation of some prochiral 3-substituted cyclobutanones using monooxygenase enzymes: a single-step method for the synthesis of optically enriched 3-substituted γ-lactones

V. Alphand, R. Furstoss, G. Grogan, 1995 .

Preparation and Determination of the Absolute Configuration of Optically Active 9-Hydroxy-7-oxabicyclo[4.3.0]non-4-en-8-ones

D. Hibbs, M. Hursthouse, K. S. Bisht, 1995 .

Some reactions of 2-azabicycio[2.2.1]hept-5-enes with diphenylketene: preparation of polysubstituted piperidin-2-ones

S. Roberts, Russell J. Thomas, Smith Colin William, 1990 .

Some unexpected reactions involving diphenylketene

S. Roberts, R. Maurya, R. J. Pryce, 1992 .

Approaches to the C-24 to C-37 perimeter of altohyrtin A

S. Roberts, Daniel J. Watson, S. Hermitage, 1998 .

Stereoselective synthesis of Z-disubstituted olefins via 2,3-sigmatropic rearrangements. An approach to leukotrienes.

S. Roberts, G. Pattenden, A. D. Kaye, 1986 .

BICYCLES, TRICYCLES AND PROSTAGLANDIN SYNTHESIS

R. Newton, S. Roberts, 1979 .

Sulphone-mediated cyclobutanone to α-alkoxy-cyclopentanone ring expansion reactions ; scope, limitations and applications

J. Montana, A. Mjalli, H. Finch, 1990 .

Novel antiparasitic agents derived by modification of a new natural product series

David J. Williams, A. Slawin, A. H. Shingler, 1987 .

Facile synthesis of (+)-brefeldin a utilizing two optically active synthons prepared by different enzyme-catalysed reactions

S. Roberts, H. Olivo, R. Mccague, 1994 .

Synthesis of optically active 5′-noraristeromycin: enzyme-catalysed kinetic resolution of 9-(4-hydroxycyclopent-2-enyl)purines

R. Storer, S. Roberts, V. Merlo, 1993 .

The potential of carbocyclic nucleosides for the treatment of AIDS: synthesis of some diphosphorylphosphonates possessing potent activity against HIV-coded reverse transcriptase

D. Coe, R. Storer, S. Roberts, 1992 .

Radical cyclisation reactions leading to polyhydroxylated cyclopentane derivatives: synthesis of (1R,2R,3S,4R)- and (1S,2S,3R,4S)-4-hydroxyethylcyclopentane-1,2,3-triol

S. Roberts, K. A. Shoberu, 1992 .

Preparation of optically pure cross-conjugated cyclopentadienones

M. Santoro, S. Roberts, M. Iqbal, 2004 .

Steric control in prostaglandin synthesis involving bicyclic and tricyclic intermediates

R. Newton, S. Roberts, 1980 .

Synthesis and antiviral activity of prostaglandin-J1 methyl ester

M. Santoro, S. Roberts, T. Guyot, 1999 .

Facile conversion of 4-endo-hydroxy-2-oxabicyclo[3.3.0]oct-7-en-3-one into carbocyclic 2′-deoxyribonucleoside analogues

S. Roberts, A. Dhanda, D. Varley, 1999 .

Potential use of carbocyclic nucleosides for the treatment of AIDS: chemo-enzymatic syntheses of the enantiomers of carbovir

C. T. Evans, S. Roberts, A. Sutherland, 1992 .

Enzymatic resolution of cis- and trans-4-hydroxycyclopent-2-enylmethanol derivatives and a novel preparation of carbocyclic 2′,3′-dideoxydidehydronucleosides and aristeromycin

S. Roberts, K. A. Shoberu, 1991 .

A route to the structure proposed for puetuberosanol and approaches to the natural products marshrin and phebalosin

S. Roberts, A. Gillmore, Christelle Lauret, 2003 .

Selective removal of the methyldiphenylsilyl protecting group using azide ion

S. Roberts, D. Parry, Steven J. Monger, 1989 .

Julia–Colonna asymmetric epoxidation of furyl styryl ketone as a route to intermediates to naturally-occurring styryl lactones

S. Roberts, Weiping Chen, 1999 .

Asymmetric epoxidation of a geminally-disubstituted and some trisubstituted enones catalysed by poly-l-leucine

A. Steiner, S. Roberts, J. Bickley, 2001 .

Improved Procedure for Julia—Colonna Asymmetric Epoxidation of α,β‐Unsaturated Ketones: Total Synthesis of Diltiazem and Taxol Side‐Chain.

S. Roberts, R. Mccague, T. Nugent, 1998 .

The semi-pinacol rearrangement of homochiral epoxyalcohols catalysed by rare earth triflates

B. Hauer, J. Skidmore, S. Roberts, 2001 .

Bicyclo[3.2.0]hept-2-en-6-one cyanohydrins: preparations by chemical hydrocyanation, and enantio- and diastereoselective biotransformation by the hydroxynitrile lyase from Prunus amygdalus in the form of almond meal

D. Hibbs, S. Coles, M. Hursthouse, 1999 .

Some recent developments in the use of enzyme catalysed reactions in organic synthesis.

N. Turner, S. Roberts, S M Roberts, 1992, Journal of biotechnology.

Carbocyclic analogues of penicllin

A. Reason, S. Roberts, O. Meth-Cohn, 1982 .

Preparative biotransformations : whole cell and isolated enzymes in organic synthesis

S. Phythian, S. Roberts, G. Casy, 1992 .

Chiral amplification by polypeptides and its relevance to prebiotic catalysis.

S. Roberts, D. Kelly, Alastair D. Meek, 2004, Chemical communications.

Enantiocomplementary total asymmetric syntheses of prostaglandin A2

D. Reynolds, R. Newton, S. Roberts, 1983 .

CHEMOENZYMATIC SYNTHESIS OF A NOVEL LIGAND FOR RHODIUM-CATALYSED ASYMMETRIC HYDROGENATION

S. Roberts, R. Mccague, R. Selke, 1997 .

Novel preparation of (−)-4-hydroxycyclohex-2-enone: reaction of 4-hydroxycyclohex-2-enone and 4-hydroxycyclopent-2-enone with some thiols

P. Evans, S. Roberts, J. Bickley, 2006 .

The Cleavage of t-Butyldimethylsilyl Ethers with Boron Trifluoride Etherate

R. Newton, S. Roberts, D. Kelly, 1979 .

A SECOND GENERATION PYRANOSE-BASED APPROACH TO THE F RING (C38-C45) OF ALTOHYRTIN A

S. Roberts, P. Kary, 1999 .

Strategies Employed in the Synthesis of Prostacyclins and Thromboxanes

R. Newton, S. Roberts, R. Taylor, 1984 .

The use of free radical cyclization in the synthesis of compounds related to the mannostatins

Peter R. Moore, S. Roberts, A. Ingall, 1994 .

Synthesis of 9-deoxy-8,9-oxaprostaglandins

M. Kelly, R. Newton, S. Roberts, 1990 .

Synthesis of (1R,2S,3R,4R)-2,3,4-trihydroxycyclopentylamine from D-ribonolactone

Peter R. Moore, S. Roberts, Ingall Anthony Howard, 1994 .

Stereocontrolled conversion of some optically active (4S,5R)-dihydroisoxazoles into acyclic 3-acetamido-1,2-diols

J. Skidmore, S. Roberts, J. Bickley, 2003 .

Total synthesis of prostaglandin D2 methyl ester

D. Reynolds, R. Newton, S. Roberts, 1980 .

S. Roberts, J. Berge, 1979 .

The Chemistry of Epoxy Alcohols

S. Roberts, Paula C. A. Pena, 2003 .

Preparation and some reactions of tricyclo[3.3.0.0]octan-2-ones and tricyclo[3.2.0.0]heptan-2-ones

R. Holt, H. Finch, M. Mahon, 1990 .

Intramolecular nucleophilic addition to photochemically generated ketenes as a versatile route to lactones and lactams; synthesis of a mosquito pheromone, goniothalamin, argentilactone, and the Streptomyces L-factor

S. Rahman, S. Roberts, M. Dowle, 1989 .

Polyhalogenoaromatic compounds. Part XIII. The reduction of pentachloropyridine and derivatives with lithium aluminium hydride and other complex metal hydrides

S. Roberts, H. Suschitzky, F. Binns, 1970 .

Synthesis and use of 7-substituted norbornadienes for the preparation of prostaglandins and prostanoids

A. Baxter, R. Newton, S. Roberts, 1986 .

Search for novel cytoprotective and antiviral prostanoids

M. Santoro, S. Roberts, 1999 .

Synthesis of prostaglandin-F2α by conjugate addition of a cuprate reagent to 3-t-butyldimethylsilyloxytricyclo[3.2.0.02,7]heptan-6-one

R. Newton, Thomas V. Lee, S. Roberts, 1977 .

β-Peptides as catalysts: poly-β-leucine as acatalyst for the Juliá–Colonna asymmetric epoxidation ofenones

J. Skidmore, S. Roberts, K. Drauz, 2001 .

Development of the biocatalytic resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one as an entry to single-enantiomer carbocyclic nucleosides

C. T. Evans, J. Littlechild, G. Ruecroft, 1993 .

Synthesis of either enantiomer of cis-3-aminocyclopentanecarboxylic acid from both enantiomers of racemic 2-azabicyclo[2.2.1]hept-5-en-3-one

C. T. Evans, S. Roberts, A. Sutherland, 1991 .

Enzyme-catalysed Baeyer–Villiger oxidations

Peter W. H. Wan, S. Roberts, Stanley M. Roberts, 1998 .

Structure and catalytic activity of some soluble polyethylene glycol–peptide conjugates

T. Bui, A. Drake, S. Roberts, 2004 .

β-Peptides as Catalysts: Poly-β-leucine as a Catalyst for the Julia—Colonna Asymmetric Epoxidation of Enones.

J. Skidmore, S. Roberts, K. Drauz, 2002 .

Lipase-catalysed Baeyer–Villiger reactions

P. Richardson, S. Roberts, S. Lemoult, 1995 .

Principles of molecular recognition

A. Buckingham, A. Legon, S. Roberts, 1993 .

Facile biocatalytic syntheses of optically active 4-hydroxycyclohex-2-enone and 4-benzylthiacyclopent-2-enone

P. Evans, S. Roberts, B. Morgan, 2004 .

Chirality and its importance in drug development: a synthetic chemist's perspective.

S. Roberts, 1991, Biochemical Society transactions.

Studies of lipase‐catalyzed polyesterification of an unactivated diacid/diol system

S. Roberts, F. Binns, Alan H. Taylor, 1998 .

Asymmetric epoxidation of some arylalkenyl sulfones using a modified Juliá-Colonna procedure

M. R. Pitts, J. López-Pedrosa, S. Roberts, 2004 .

Asymmetric Epoxidation of Some Arylalkenyl Sulfones Using a Modified Julia—Colonna Procedure.

M. R. Pitts, J. López-Pedrosa, S. Roberts, 2004 .

Stereocontrolled ring-opening of some enantiomerically enriched epoxy ketones and epoxy alcohols using trimethylaluminium: synthesis of (S)-2-arylpropanoic acids

S. Roberts, Lydia Carde, D. Davies, 2000 .

Enantiocomplementary asymmetric epoxidation of selected enones using poly-L-leucine and poly-D-leucine

S. Roberts, M. Sanchez, 1995 .

PaaSiCats: novel polyamino acid catalysts.

S. Roberts, A. Dhanda, K. Drauz, 2000, Chirality.

Unexpected asymmetric epoxidation reactions catalysed by polyleucine-based systems

P. Mayon, W. Kroutil, S. Roberts, 1996 .

Development of the juliá asymmetric epoxidation reaction. Part 1. Application of the oxidation to enones other than chalcones

P. Mayon, S. Roberts, S. R. Thornton, 1996 .

Enantiocomplementary Asymmetric Epoxidation of Selected Enones Using Poly-L-leucine and Poly-D-leucine.

S. Roberts, M. Sanchez, 1995 .

Enantioselective epoxidation of chalcone catalysed by the artificial enzyme poly-l-leucine: kinetic mechanism

S. Colonna, G. Carrea, G. Ottolina, 2004 .

Stereocontrolled Ring-Opening of Some Enantiomerically Enriched Epoxy Ketones and Epoxy Alcohols Using Trimethylaluminum: Synthesis of (S)-2-Arylpropanoic Acids.

S. Roberts, Lydia Carde, D. Davies, 2000 .

Enzyme-catalysed hydrolyses of some meso-diesters

A. Drake, G. Ryback, V. Šik, 1991 .

Reduction of Bicyclo[3.2.0]hept-2-en-6-one and 7,7-Dimethylbicyclo[3.2.0]hept- 2-en-6-one Using Dehydrogenase Enzymes and the Fungus Mortierella ramanniana.

W. F. Wall, M. Turner, M. Dawson, 1986 .

Reduction of 7-chlorobicyclo[3.2.0]hept-2-en-6-ones catalysed by 3α,20β-hydroxysteroid dehydrogenase

M. Turner, S. Roberts, J. Leaver, 1986 .

Oxidative biotransformations by microorganisms: production of chiral synthons by cyclopentanone monooxygenase fromPseudomonas sp. NCIMB 9872

M. Bes, R. Villa, S. Roberts, 1996 .

Investigation of the regioselectivity of some esterifications involving methyl 4,6-O-benzylidene D-pyranosides and Pseudomonas fluorescens lipase

G. Iacazio, S. Roberts, 1993 .

Regioselective enzymatic acetylation of methyl 4,6-O-benzylidene-α- and β-D-glucopyranoside

M. Chinn, N. Turner, S. Roberts, 1992 .

Enzymatic resolution of sterically demanding bicyclo[3.2.0]heptanes: evidence for a novel hydrolase in crude porcine pancreatic lipase and the advantages of using organic media for some of the biotransformations

K. Faber, S. Roberts, A. Sutherland, 1991 .

Preparation of neplanocin-A from D-ribose and by a chemoenzymic method

N. Turner, S. Roberts, D. Grand, 1994 .

Enzyme-catalysed hydrolysis of dimethyl 7-hydroxy-3,3-dimethyl-2,4-dioxabicyclo[3.3.0]octane-6,8-dicarboxylate and a novel synthesis of neplanocin A

S. Roberts, E. J. Hutchinson, A. Thorpe, 1992 .

Synthesis and Rearrangement of 7-Halobicyclo[3.2.0]hept-2-en-6-ols

S. Roberts, J. Griffiths, A. Dreiding, 1977 .

Some Recent Studies into the Use of Enzymes in Organic Synthesis

N. Turner, S. Roberts, A. Willetts, 1993, CHIMIA.

Chemoenzymatic synthesis of some macrocyclic C13-lactones

M. Mahon, V. Šik, S. Roberts, 1991 .

Chemo-Enzymatic Synthesis of 13-S-Hydroxyoctadecadienoic Acid (13-S-HODE)

S. Roberts, Philip B Cox, C. Chan, 1990 .

The synthesis of (R)-(+)-lipoic acid using a monooxygenase-catalysed biotransformation as the key step.

M. Bes, R. Villa, G. Grogan, 1997, Bioorganic & medicinal chemistry.

Application of enzymic Baeyer–Villiger oxidations of 2-substituted cycloalkanones to the total synthesis of (R)-(+)-lipoic acid

M. Bes, R. Villa, G. Grogan, 1995 .

Synthetic approaches towards nucleocidin and selected analogues; anti-HIV activity in 4′-fluorinated nucleoside derivatives

Anita R. Maguire, Andrew Willetts, A. Maguire, 1993 .

An efficient protocol for the stereoselective dihydroxylation of ene-ester systems

P. Nielsen, S. Roberts, S. Hermitage, 1998 .

Titanium mediated alkylidenation of substituted cycloalkenones: scope and limitations

S. Roberts, Alan M. Happe, J. Dauvergne, 2004 .

Synthesis of 4-azacyclopent-2-enones and 5,5-dialkyl-4-azacyclopent-2-enones

M. R. Pitts, T. Snape, S. Singh, 2004 .

Use of polymer supported thiophenol for the synthesis and purification of a benzimidazol-2-one library

J. Montana, A. Baxter, S. Roberts, 2000 .

Fluorocarbocyclic nucleosides: synthesis and antiviral activity of 2'- and 6'-fluorocarbocyclic 2'-deoxy guanosines.

S. Roberts, J. Coates, D. Ryan, 1991, Journal of medicinal chemistry.

Biosynthesis of aristeromycin: the role of (1R, 2R, 3S, 4S)-1-hydroxymethylcyclopentane-2,3,4-triol

J. Hanrahan, E. Wellington, S. Roberts, 1994 .

Conversion of (–)-4-hydroxy-2-oxabicyclo[3.3.0]oct-7-en-3-one into the anti-HIV agent carbovir

S. Roberts, H. Olivo, R. Mccague, 1993 .

Synthesis of carbocyclic clitocine

S. Roberts, K. Parry, C. F. Palmer, 1990 .

Fluoro carbocyclic nucleosides: synthesis and antiviral activity of 2'- and 6'-fluoro carbocyclic pyrimidine nucleosides including carbocyclic 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-methyluracil and carbocyclic 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodouracil.

S. Roberts, J. Coates, B. E. Kirk, 1990, Journal of medicinal chemistry.

Synthesis and enzymatic resolution of carbocyclic 2′-ara-fluoro-guanosine: a potent new anti-herpetic agent

J. Cameron, S. Roberts, B. E. Kirk, 1988 .

Use of diethylaminosulphur trifluoride (DAST) in the preparation of synthons of carbocyclic nucleosides

S. Roberts, B. E. Kirk, A. D. Borthwick, 1988 .

Synthesis and biological activity of the diphosphorylphosphonate derivatives of (+)- and (–)-cis-9-(4′-hydroxycyclopent-2′-enyl)guanine

R. Bethell, R. Storer, S. Roberts, 1994 .

Synthesis of two 6′α-fluorocarbocyclic nucleosides and incorporation into short segments of DNA

S. Roberts, A. N. Payne, 1992 .

Chemoenzymatic synthesis of (–)-carbovir utilizing a whole cell catalysed resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one

Steven J Taylor, C. Evans, S. Roberts, 1990 .

Synthesis and Enzymatic Resolution of Carbocyclic 2′-Ara-fluoroguanosine (I): A Potent New Anti-Herpetic Agent.

J. Cameron, S. Roberts, B. E. Kirk, 1988 .

Chemoenzymatic synthesis of carbocyclic oxetanocin-A involving a novel photochemical rearrangement

S. Roberts, I. Cotterill, 1992 .

Synthesis of Carbocyclic Clitocine.

S. Roberts, K. Parry, C. F. Palmer, 1990 .

Use of Diethylaminosulfur Trifluoride (DAST) in the Preparation of Synthons of Carbocyclic Nucleosides.

S. Roberts, B. E. Kirk, A. D. Borthwick, 1988 .

Synthesis and Biological Activity of the Diphosphorylphosphonate Derivatives of (+)‐ and (‐)‐cis‐9‐(4′‐Hydroxycyclopent‐2′‐enyl)guanine.

R. Bethell, R. Storer, S. Roberts, 1994 .

Overcoming intrinsic diastereoselection using polyleucine as a chiral epoxidation catalyst

S. Roberts, P. Ray, 1999 .

Synthesis of monohydroxylated 2-azabicyclo[2.2.1]heptan-3-ones

S. Roberts, A. Willetts, R. Mccague, 1997 .

Synthesis of Two 6′α‐Fluorocarbocyclic Nucleosides and Incorporation into Short Segments of DNA.

S. Roberts, A. N. Payne, 1993 .

The potential for using carbocyclic nucleosides for the treatment of AIDS. Part 1. Preparation of some analogues for azidothymidine (AZT)

R. Storer, H. Hilpert, S. Roberts, 1991 .

Factors governing the ratio of isomeric oxabicyclo[3.2.1]octanones formed on Baeyer–Villiger oxidation of some 5-endo,7-anti-disubstituted bicyclo[2.2.1]heptan-2-ones

R. Newton, S. Roberts, C. C. Howard, 1978 .

Electrophilic bromination of bicyclo[3.2.0]hept-2-en-6-ones

S. Roberts, Z. Grudzinski, 1975 .

Chemoenzymatic Synthesis of (‐)‐Carbovir Utilizing a Whole Cell‐ Catalyzed Resolution of 2‐Azabicyclo(2.2.1)hept‐5‐en‐3‐one.

C. T. Evans, S. Roberts, A. Sutherland, 1991 .

Short convergent route to homochiral carbocyclic-2′-deoxynucleosides and carbocyclic ribonucleosides

S. Roberts, B. E. Kirk, A. D. Borthwick, 1987 .

Chemoenzymatic Synthesis of Carbocyclic Oxetanocin-A Involving a Novel Photochemical Rearrangement.

S. Roberts, I. Cotterill, 1993 .

Modified triphosphates of carbocyclic nucleoside analogues: Synthesis, stability towards alkaline phosphatase and substrate properties for some DNA polymerases

A. Krayevsky, S. Roberts, F. Theil, 1996 .

Synthesis of fluorinated carbocyclic nucleosides: preparation of carbocyclic 1-(2′-deoxy-6′-fluororibofuranosyl)-5-iodouracils

A. Slawin, S. Roberts, B. E. Kirk, 1987 .

SYNTHESIS OF THE PHOSPHONATE ISOSTERE OF CARBOCYCLIC 5-BROMOVINYLDEOXYURIDINE MONOPHOSPHATE

A. Garofalo, D. Coe, R. Storer, 1994 .

The synthesis of new adenosine A3 selective ligands containing bioisosteric isoxazoles.

C. Thomsen, S. Roberts, L. Knutsen, 1998, Bioorganic & medicinal chemistry letters.

SOLID-PHASE SYNTHESIS OF OLIGODEOXYNUCLEOTIDES CONTAINING 3′-S-PHOSPHOROTHIOLATE LINKAGES

S. Roberts, I. O'neil, R. Cosstick, 2001, Nucleosides, nucleotides & nucleic acids.

New Synthetic Routes to Prostaglandins and Thromboxanes

S. Roberts, F. Scheinmann, 1982 .

Overcoming Intrinsic Diastereoselection Using Polyleucine as a Chiral Epoxidation Catalyst.

S. Roberts, P. Ray, 1999 .

Synthesis of some carbocyclic nucleoside analogues based on a bicyclo[3.1.0]hexane ring system

H. Gooding, R. Storer, S. Roberts, 1994 .

Modified nucleoside 5'-triphosphonates as a new type of antiviral agents.

R. Beabealashvilli, A. Krayevsky, C. Hamilton, 1999, Nucleosides & nucleotides.

Synthesis of Fluorinated Carbocyclic Nucleosides: Preparation of (.+-.)-Carbocyclic-FMAU and Some Congeners.

A. Slawin, S. Roberts, B. E. Kirk, 1987 .

Stereoselective conversion of 2′,3′-dideoxydidehydro carbocyclic nucleosides into 2′-deoxy carbocyclic nucleosides

S. Roberts, A. Dhanda, D. Varley, 1998 .

Synthesis of Monohydroxylated 2-Azabicyclo(2.2.1)heptan-3-ones.

S. Roberts, A. Willetts, R. Mccague, 1997 .

Rearrangement of 2-azabicyclo[2.2.1]hept-5-en-3-ones : synthesis of cis-3-aminocyclopentane carboxylic acid derivatives

V. Šik, S. Roberts, K. Parry, 1992 .

The Potential for Using Carbocyclic Nucleosides for the Treatment of AIDS. Part 1. Preparation of Some Analogues for Azidothymidine (AZT).

R. Storer, H. Hilpert, S. Roberts, 1991 .

Electrophilic substitution of a 2-azabicyclo[2.2.1]hept-5-en-3-one as a potential route to 3-deoxycarbocyclic nucleosides

S. Roberts, K. Parry, C. F. Palmer, 1991 .

Short Convergent Route to Homochiral Carbocyclic 2′-Deoxynucleosides and Carbocyclic Ribonucleosides.

S. Roberts, B. E. Kirk, A. D. Borthwick, 1988 .

Modified Triphosphates of Carbocyclic Nucleoside Analogues: Synthesis, Stability Towards Alkaline Phosphatase and Substrate Properties for Some DNA Polymerases.

A. Krayevsky, S. Roberts, F. Theil, 1997 .

Synthesis of Fluorinated Carbocyclic Nucleosides: Preparation of Carbocyclic 1-(2′-Deoxy-6′-fluororibofuranosyl)-5-iodouracils.

A. Slawin, S. Roberts, B. E. Kirk, 1987 .

Use of Microorganisms for the Resolution of Synthetically Useful Bicyclo[3.2.0]Hept-2-En-6-Ones

S. Roberts, 1986 .

Synthesis of the Phosphonate Isostere of Carbocyclic 5‐ Bromovinyldeoxyuridine Monophosphate.

A. Garofalo, D. Coe, R. Storer, 1995 .

The chemistry of compounds derived by microbial oxidation of benzene and derivatives: cycloadditions involving 1,2-isopropylidenedioxycyclohexadienes

G. Ryback, M. Mahon, V. Šik, 1991 .

Diels-Alder reactions involving 1,2-isopropylidenedioxy-3-trifluoromethylcyclohexa-3,5-diene

G. Ryback, V. Šik, S. Roberts, 1989 .

Diels–Alder reactions involving cis-1,2-isopropylidenedioxycyclohexa-3,5-diene and enzymatic resolution of one of the adducts

S. Roberts, I. Cotterill, Julian O. Williams, 1988 .

Reaction of diphenylketene with some cyclohexa-3,5-diene-1,2-cis-diol derivatives: conversion of chlorobenzene into optically active 2-oxabicyclo[2.2.2]octen-3-one

S. Roberts, Julian O. Williams, P. W. Sutton, 1994 .

[4 + 2], [2 + 2], and Carbene addition reactions involving cyclohexa-3,5-diene-cis-1,2-diol derivatives

G. Ryback, S. Roberts, R. J. Pryce, 1990 .

The Chemistry of Compounds Derived by Microbial Oxidation of Benzene and Derivatives: Cycloadditions Involving 1,2- Isopropylidenedioxycyclohexadienes.

G. Ryback, M. Mahon, V. Šik, 1991 .

Diels-Alder Reactions Involving cis-1,2-Isopropylidenedioxycyclohexa-3,5-diene and Enzymatic Resolution of One of the Adducts.

S. Roberts, I. Cotterill, Julian O. Williams, 1989 .

(4 + 2), (2 + 2), and Carbene Addition Reactions Involving Cyclohexa-3,5-diene-cis-1,2-diol Derivatives.

G. Ryback, S. Roberts, R. J. Pryce, 1990 .

Reaction of Diphenylketene with Some Cyclohexa‐3,5‐diene‐1,2‐cis‐diol Derivatives: Conversion of Chlorobenzene into Optically Active 2‐ Oxabicyclo(2.2.2)octen‐3‐ones.

S. Roberts, Julian O. Williams, P. W. Sutton, 1994 .

Reactions of diphenylketene and methylphenylketene with some cis-cyclohexa-3,5-diene-1,2-diol derivatives

S. Roberts, L. Wright, P. W. Sutton, 1996 .

Reactions of some substituted isoxazoles with organolithium reagents

S. Roberts, J. Gainer, H. Suschitzky, 1976 .

Novel aliphatic epoxide hydrolase activities from dematiaceous fungi.

G. Grogan, S. Roberts, A. Willetts, 1996, FEMS microbiology letters.

Photolysis of 2,3-epoxy-7,7-diphenylbicyclo[3.2.0]heptan-6-ones and 2-exo, 3-exo-dihydroxy-7,7-diphenylbicyclo[3.2.0]heptan-6-one

S. Rahman, S. Roberts, B. Wakefield, 1987 .

SOME STEREOCONTROLLED REACTIONS OF BICYCLO(3.2.0)HEPTAN-6-ONES AND 2-OXABICYCLO(3.3.0)OCTAN-3-ONES

R. Newton, Thomas V. Lee, S. Roberts, 1979 .

Chemistry, biochemistry, and pharmacological activity of prostanoids

S. Roberts, F. Scheinmann, 1979 .

Guide to organic stereochemistry

S. Roberts, Sheila R. Buxton, Stanley M. Roberts, 1996 .

Biomimetic reactions in organic synthesis: Semi-pinacol rearrangements of some spirocyclic epoxyalcohols derived from Juliá-Colonna asymmetric epoxidations

John Skidmore, Bernhard Hauer, B. Hauer, 2002 .

Titanium-substituted zeolite beta: an efficient catalyst in the oxy-functionalisation of cyclic alkenes using hydrogen peroxide in organic solvents

G. Hutchings, E. Derouane, S. Roberts, 1998 .

Three-step synthesis of α-methylene-γ-lactones through formation and oxidation of substituted cyclobutanones

S. Roberts, S. Ali, 1976 .

Induction of Apoptosis in Estrogen Receptor-Negative Breast Cancer Cells by Natural and Synthetic Cyclopentenones: Role of the IκB Kinase/Nuclear Factor-κB Pathway

T. Snape, R. Piva, A. Ciucci, 2006, Molecular Pharmacology.

Biocatalysis and biotransformation: Probing the potential usefulness and the mechanisms of action of some novel biocatalysts

B. Hauer, S. Roberts, 2004 .

The norbornadiene route to prostaglandin I2 and other prostaglandins: preparation and rearrangement of 7-substituted norbornadienes

A. Baxter, R. Newton, S. Roberts, 1983 .

PUTTING MICROBES TO WORK

S. Roberts, A. Carnell, 1997 .

Molecular recognition : chemical and biochemical problems II

S. Roberts, Stanley M. Roberts, 1992 .

Preparation of optically active cyclohexanediols and (+)-α- hydroxycycloheptanone by an enzyme catalysed stereoinversion/oxidation process

G. Iacazio, S. Roberts, A. Willetts, 1994 .

Enzyme-catalysed hydrolysis of 3,5-cis-diacetoxy-4-trans-benzyloxy-methylcyclopentene and the synthesis of aristeromycin precursors

S. Roberts, D. Legrand, 1992 .

Total synthesis of prostaglandin-F2 alpha involving stereocontrolled and photo-induced reactions of bicyclo[3.20]heptanones.

D. Reynolds, R. Newton, S. Roberts, 1980, Journal of the Chemical Society. Perkin transactions 1.

Regio- and stereo-controlled oxidations and reductions

S. Roberts, J. Whittall, 2007 .

Selective Biohydroxylation of 1-Substituted Adamantanes Using Absidia cylindrospora (I.M.I. 342950).

G. Rosair, P. Bailey, S. Roberts, 1996 .

Selcetive biohydroxylation of 1-substituted adamantanes using Absidia cylindrospora(I.M.I. 342950)

C. Ridyard, G. Rosair, P. Bailey, 1996 .

Synthesis and Revision of the Stereochemistry of a Cyclopentenone Natural Product Isolated from Ascomycete Strain A23-98.

T. Snape, M. Santoro, S. Roberts, 2004 .

Peroxy-acid oxidation of NN-disubstituted aminotetrafluoro-, amino-3-chlorotrifluoro-, and amino-3,5-dichlorodifluoro-pyridines

S. Roberts, H. Suschitzky, 1969 .

Induction of Apoptosis in Estrogen-Receptor Negative Breast Cancer Cells by Natural and Synthetic Cyclopentenones : Role of the IKK / NF-κ B Pathway

R. Piva, A. Ciucci, M. Santoro, 2006 .

Polyamino Acids as Man-Made Catalysts

S. Roberts, Joanne V. Allen, N. Williamson, 1999 .

A novel fluoride induced cyclisation reaction

S. Roberts, S. Hermitage, 1998 .

Stereoselective epoxidation of electron poor dienes using poly(L-leucine)

S. Roberts, Joanne V. Allen, N. Williamson, 1997 .

Reactions of ethyl 2-acetyl-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylate and 4-acetylamino-2-oxabicyclo[3.3.0]oct-7-en-3-one with some electrophiles

D. Hibbs, M. Hursthouse, R. Storer, 1995 .

Biotransformation of alkenes by haloperoxidases: Regiospecific bromohydrin formation from cinnamyl substrates

S. Roberts, A. Willetts, P. Coughlin, 1993, Biotechnology Letters.

New preparative routes to isosorbide 5-mononitrate

S. Roberts, P. Quigley, Christopher M. Brown, 2000 .

New Preparative Routes to Isosorbide 5-Mononitrate.

S. Roberts, P. Quigley, Christopher M. Brown, 2000 .

Novel rearrangement of a cephalosporin into a trisubstituted thiazole

K. Henrick, P. G. Owston, S. Roberts, 1983 .

Stereochemical congruence of Baeyer–Villigerases

C. Knowles, M. A. Wright, G. Grogan, 1996 .

Total synthesis of prostaglandin-F2α through homoconjugate addition of an organocuprate reagent to a tricyclo[3.2.0.02,7]heptanone

R. Newton, Thomas V. Lee, S. Roberts, 1978 .

The Use of Enzymes for the Preparation of Biologically Active Natural Products and Analogues in Optically Active Form

S. Roberts, N. Williamson, 1997, Current Organic Chemistry.