E. J. Thomas

发表

C.-C. Tseng, David Young, Nobuhiro Takeda, 2003 .

Synthesis of 5-hydroxy-2,3,4,5-tetrahydro-[1H]-2-benzazepin-4-ones: selective antagonists of muscarinic (M3) receptors.

E. J. Thomas, B. Bradshaw, P. Evans, 2008, Organic & biomolecular chemistry.

Synthesis of chiral organotin reagents: synthesis of enantiomerically enriched bicyclo[2.2.1]hept-2-yl tin hydrides from camphor. X-Ray crystal structures of (dimethyl)[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]tin chloride and methyl(phenyl)bis[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2

E. J. Thomas, M. Helliwell, Linda A. Townsend, 2002 .

Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition

E. J. Thomas, Duncan M. Gill, Nicholas H. Taylor, 2011 .

Total synthesis of a 20-deoxybryostatin.

E. J. Thomas, A. Green, Alan T. L. Lee, 2011, Chemical communications.

Synthesis of the C(1)–C(16) fragment of bryostatins using an ‘ene’ reaction between an allylsilane and an alkynone

E. J. Thomas, M. O’Brien, 2011 .

Approaches to the total synthesis of biologically active natural products: studies directed towards bryostatins

E. J. Thomas, A. Green, Alan T. L. Lee, 2010, Phytochemistry Reviews.

On the use of the modified Julia olefination for bryostatin synthesis

E. J. Thomas, A. Green, Alan T. L. Lee, 2008 .

Stereoselective thermal reactions between (E)-1-alkoxymethoxybut-2-enyl-(tributyl)stannanes and aldehydes

E. J. Thomas, A. Pratt, 1989 .

Structure-Based Design of MptpB Inhibitors That Reduce Multidrug-Resistant Mycobacterium tuberculosis Survival and Infection Burden in Vivo

E. J. Thomas, L. Tabernero, Ajanta Chakraborty, 2018, Journal of medicinal chemistry.

Stereoselective synthesis of allylic amines by rearrangement of allylic trifluoroacetimidates: stereoselective synthesis of polyoxamic acid and derivatives of other α-amino acids

E. J. Thomas, P. D. Wilson, Ian Savage, 1999 .

Asymmetric α-aminoacid synthesis using [3.3] rearrangement of allylic trifluoroacetimidates: Synthesis of thymine polyoxin C

E. J. Thomas, Anqi Chen, Ian Savage, 1993 .

Systematic Comparison of Sets of 13C NMR Spectra That Are Potentially Identical. Confirmation of the Configuration of a Cuticular Hydrocarbon from the Cane Beetle Antitrogus parvulus

E. J. Thomas, G. Morris, K. Damodaran, 2014, The Journal of organic chemistry.

Total syntheses of epothilones B and D: applications of allylstannanes in organic synthesis

Nathaniel G. Martin, E. J. Thomas, E. Thomas, 2001 .

Synthesis and absolute configuration of optically active E-1-alkoxymethoxy-but-2-eny(tri-n-butyl)stannanes: stereoselective reactions with aldehydes

E. J. Thomas, A. Pratt, V. J. Jephcote, 1984 .

Milbemycin synthesis : synthesis of 6β-hydroxy-3,4-dihydromilbemycin E

E. J. Thomas, E. Parmee, S. Karim, 1991 .

On the origin of 1,5-induction in tin(IV) halide-promoted reactions of 4-alkoxyalk-2-enylstannanes with aldehydes

E. J. Thomas, M. Vincent, L. Hobson, 1998 .

Synthesis of the C1 – C16 fragment of bryostatin for incorporation into 20,20-fluorinated analogues

E. J. Thomas, Paul R. Mears, E. Thomas, 2021 .

Towards 20,20-difluorinated bryostatin: synthesis and biological evaluation of C17,C27-fragments.

Claire E. Rye, E. J. Thomas, P. Eyers, 2019, Organic & biomolecular chemistry.

Synthetic approaches to the C11-C27 fragments of bryostatins.

E. J. Thomas, A. Green, Simon Hardy, 2017, Organic & biomolecular chemistry.

Total synthesis of 7-des-O-pivaloyl-7-O-benzylbryostatin 10.

E. J. Thomas, A. Green, Alan T. L. Lee, 2017, Organic & biomolecular chemistry.

Synthesis of vinylic iodides for incorporation into the C17-C27 fragment of bryostatins

E. J. Thomas, Thomas J. Gregson, E. Thomas, 2017 .

Syntheses of C17-C27 fragments of 20-deoxybryostatins for assembly using Julia and metathesis reactions.

E. J. Thomas, Thomas J. Gregson, Matthew Ball, 2017, Organic & biomolecular chemistry.

Some limitations of an approach to the assembly of bryostatins by ring-closing metathesis.

E. J. Thomas, Raphael Dumeunier, Thomas J. Gregson, 2017, Organic & biomolecular chemistry.

The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins.

E. J. Thomas, Raphael Dumeunier, B. Bradshaw, 2016, Organic & biomolecular chemistry.

Total synthesis of pamamycin 607: applications of remote asymmetric induction in organic synthesis

E. J. Thomas, O. Germay, N. Kumar, 2001 .

An approach to the C(10)–C(16) fragment of the bryostatins: stereoselective exocyclic double-bond formation by vinyl radical cyclization

E. J. Thomas, R. Maguire, S. Munt, 1998 .

Approaches to a synthesis of galbonolide B

E. J. Thomas, P. M. Smith, 1998 .

CONTROL AND APPLICATIONS OF REMOTE ASYMMETRIC INDUCTION USING ALLYLMETAL REAGENTS

E. J. Thomas, 1997 .

Asymmetric synthesis of milbemycin and avermectin spiroacetals

E. J. Thomas, P. Steel, E. Merifield, 1987 .

Asymmetric synthesis of the spiroacetal fragment of milbemycin E

Nicholas A. Stacey, E. J. Thomas, P. Steel, 1987 .

Total synthesis of epothilones using functionalised allylstannanes for remote stereocontrol.

Nathaniel G. Martin, E. J. Thomas, E. Thomas, 2012, Organic & biomolecular chemistry.

An approach to aliphatic 1,8-stereocontrol: diastereoselective syntheses of (±)-patulolide C and (±)-epipatulolide C.

E. J. Thomas, E. Hoegenauer, E. Thomas, 2012, Organic & biomolecular chemistry.

REMOTE ASYMMETRIC INDUCTION USING ALLYLSTANNANES

E. J. Thomas, 1996 .

1,5-Asymmetric induction in reactions of δ-alkoxyallylstannanes: stereoselective reactions with chiral aldehydes

E. J. Thomas, A. Mcneill, 1992 .

On the stereoselectivity of reaction between α-methylbut-2-enylstannanes and aldehydes

E. J. Thomas, S. Mortlock, C. Hull, 1989 .

An observation of diastereoface selectivity in thermal reactions between δ-alkoxyallylstannanes and aldehydes

E. J. Thomas, S. Mortlock, 1988 .

Stereoselective synthesis of Z-alkenes from α-methylcrotylstannanes and aldehydes

E. J. Thomas, S. Mortlock, C. Hull, 1987 .

Regioselective synthesis of α-substituted allyl- and homoallyl-stannanes by selenoxide elimination

E. J. Thomas, V. J. Jephcote, E. Thomas, 1985 .

Aspects of nitrile oxide cycloaddition stereoselectivity: Chemistry of 4-cyano-2,2-dimethyl- and 4-cyano-2,2,5,5-tetramethyl-1,3-dioxolane oxides. X-ray structure of (4 RS, 5RS)-4,5-bismethoxy-carbonyl-3-[(4RS)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]-Δ2-isox-azoline

E. J. Thomas, Richard H. Jones, G. C. Robinson, 1984 .

Total synthesis of AI-77-B

E. J. Thomas, J. Rexhausen, Simon D. Broady, 1991 .

Syntheses of thunbergols and α- and β-cembra-2,7,11-triene-4,6-diols

E. J. Thomas, P. Astles, 1997 .

Synthesis of chiral organotin reagents: synthesis of bicyclo[2.2.1]heptan-2-yl(diphenyl)tin hydrides with cis-disposed, oxygen-containing substituents

E. J. Thomas, R. Pratt, 1998 .

Synthesis of chiral organotin reagents: synthesis of diphenyl- {(1S,2R,3S,4R)-3-(alkoxymethyl)bicyclo[2.2.1]heptan-2-yl}tin hydrides. X-Ray crystal structure of (R)-4,4-dimethyl-2-oxotetrahydrofuran-3-yl (1S,2S,3R,4R)-3-triphenylstannylbicyclo[2.2.1]hept-5-ene-2-carboxylate

E. J. Thomas, R. L. Beddoes, R. Pratt, 1998 .

Approaches to 3,4,5-substituted piperidines via 1,2,5,6-tetrahydropyridines prepared by ring-closing metathesis

E. J. Thomas, Maxime G. P. Buffat, E. Thomas, 2016 .

1,8-Stereocontrol by 1,5-induction using an allylstannane followed by a 2,3-Wittig rearrangement: Diastereoselective total synthesis of (±)-epipatulolide C

E. J. Thomas, Andrew P Thomas, E. Dorling, 1999 .

1,8-Stereocontrol by 1,5-induction using an allylstannane followed by Ireland-Claisen rearrangement: Diastereoselective total synthesis of (±)-patulolide C

E. J. Thomas, E. Dorling, Eric J. Thomas, 1999 .

1,6-Asymmetric induction in reactions between 6-hydroxy-5-methylhex-2-enyl(tributyl)stannane and aldehydes promoted by tin(IV) bromide

E. J. Thomas, S. Stanway, 1995 .

1,6-asymmetric induction in Lewis acid promoted reactions of ε-methoxy- and ε-hydroxy-allylstannanes and aldehydes

E. J. Thomas, J. S. Carey, 1993 .

Synthesis of optically active (E)-1-alkoxymethoxybut-2-enyl(tributyl)stannanes: stereochemistry of their thermal reactions with aldehydes

E. J. Thomas, A. Pratt, V. J. Jephcote, 1989 .

1,5-Stereocontrol in reactions of 5-benzyloxy-4-methylpent-2-enyl bromides with aldehydes mediated by Bi(0): synthesis of aliphatic compounds with 1,5-syn-related methyl groups

E. J. Thomas, M. Fielding, Sam Donnelly, 2004 .

Aspects of the chemistry of dioxolanes: Synthesis of C-nucleoside analogues

E. J. Thomas, B. Mellor, Patricia E. Murray, 1998 .

Development of a synthesis of lankacidins: synthesis of the C(14)–C(6) fragment and introduction of the C(10)–C(13) diene

E. J. Thomas, Jane M. Roe, 1995 .

Synthesis of macrocyclic precursors of the vioprolides.

E. J. Thomas, A. Regan, Gonzalo Gómez-Campillos, 2018, Organic & biomolecular chemistry.

Synthesis of the (E)-dehydrobutyrine–thiazoline–proline–leucine fragment of vioprolides B and D

E. J. Thomas, Hao Liu, 2013 .

Total synthesis of AI-77-B: stereoselective hydroxylation of 4-alkenylazetidinones

E. J. Thomas, J. Rexhausen, Simon D. Broady, 1999 .

Synthesis of macrocyclic precursors of lankacidins using Stille reactions of 4-(2-iodo-alkenyl)azetidinones and related compounds for ring closure

E. J. Thomas, A. Nelson, Anqi Chen, 2010 .

Stereoselective synthesis of oxazolidinonyl-fused piperidines of interest as selective muscarinic (M1) receptor agonists: a novel M1 allosteric modulator.

E. J. Thomas, E. Burnell, R. Davies, 2016, Organic & biomolecular chemistry.

1,5-Asymmetric induction in reactions betweenδ-alkoxyallylstannanes and aldehydes induced by tin (IV) chloride

E. J. Thomas, A. Mcneill, 1990 .

Remote asymmetric induction in reactions between 4- and 5-benzyloxypent-2-enyl(tributyl)stannanes and chiral imines prepared from butyl glyoxylate

E. J. Thomas, D. Hallett, E. Thomas, 1995 .

Stereospecificity in Reactions of Allylstannanes with Aldehydes Explored by Electronic Structure Calculations.

Richard J. Hall, E. J. Thomas, M. Vincent, 1999, The Journal of organic chemistry.

Concerning the 1,5-stereocontrol in tin(IV) chloride promoted reactions of 4- and 5-alkoxyalk-2-enylstannanes: trapping intermediate allyltin trichlorides using phenyllithium.

E. J. Thomas, L. Hobson, 2012, Organic & biomolecular chemistry.

Remote stereocontrol in reactions between 4- and 5-alkoxyalk-2-enylstannanes and 1-alkoxycarbonylimines and analogues: stereoselective approaches to novel α-amino acids.

E. J. Thomas, D. Hallett, N. Tanikkul, 2012, Organic & biomolecular chemistry.

1,5-Stereocontrol in tin(IV) halide mediated reactions between N- and S-substituted pent-2-enylstannanes and aldehydes or imines

E. J. Thomas, S. Stanway, 2012 .

Effective 1,5-, 1,6- and 1,7-remote stereocontrol in reactions of alkoxy- and hydroxy-substituted allylstannanes with aldehydes.

E. J. Thomas, J. S. Carey, S. Stanway, 2011, Organic & biomolecular chemistry.

Stereochemical aspects of the chemistry of 2-[trialkyl(aryl)silyloxy]alkyl-4-alkoxyalk-2-enylstannanes

E. J. Thomas, Daniel R. Tray, 2011 .

Applications of remote stereocontrol using allylstannanes: an approach to the stereoselective synthesis of aliphatic polyols

E. J. Thomas, A. Mcneill, 2011 .

1,5-Stereocontrol in tin(IV) halide promoted reactions of 2-alkoxy-1-(2-tributylstannylethylidene)cyclohexanes with aldehydes

E. J. Thomas, Poonam C. Kumar, Daniel R. Tray, 2007 .

1,5-Remote stereocontrol using allylgermanes

E. J. Thomas, P. Castreño, Anna P. Weston, 2007 .

1,6-Remote stereocontrol using allylgermanes

E. J. Thomas, Anna P. Weston, 2007 .

Remote stereocontrol using functionalized allylmetal reagents.

E. J. Thomas, 2007, Chemical record.

Remote stereocontrol using (E)-6-hydroxy-4-methylhex-2-enyl(tri-n-butyl)stannane

E. J. Thomas, Somhairle Maccormick, 2006 .

15-asymmetric induction in reactions between (alkoxyallyl)stannanes and aldehydes: Influence of the Lewis acid and -substituent

E. J. Thomas, J. S. Carey, T. Coulter, 1993 .

Stereoselective synthesis of aliphatic 1,5,9,13-polyols using (δ-alkoxyallyl)stannanes

E. J. Thomas, A. Mcneill, 1993 .

Remote stereocontrol using allylstannanes: reversal in stereoselectivity using indium(III) and bismuth(III) halides as promoters.

E. J. Thomas, E. A. Arnott, Sam Donnelly, 2003, Chemical communications.

Stereocontrolled syntheses of 2,5-disubstituted tetrahydrofurans using remote asymmetric induction

E. J. Thomas, L. Hobson, L. Singh, 2001 .

1,5-Asymmetric induction in reactions between 4- and 5-alkoxypent-2-enyl(tributyl)stannanes and achiral 1-alkoxycarbonylimines

E. J. Thomas, D. Hallett, 1995 .

The Effect of a tert-butyldimethylsilyl substituent on the 1,5-asymmetric induction found in reactions of 4- and 5-alkoxyallylstannanes with aldehydes and imines

E. J. Thomas, D. Hallett, G. Bradley, 1995 .

Effective 1,5-Asymmetric Induction in Tin(IV) Chloride Promoted Reactions Between Aldehydes and (4-Alkoxy-2-alkenyl)tributylstannanes

E. J. Thomas, A. Mcneill, 1994 .

1,5-Induction in reactions between 4-aminoallylstannanes and aldehydes promoted by Lewis acids

E. J. Thomas, S. Stanway, 1994 .

1,5-Asymmetric induction in Lewis acid-promoted reactions of (5-alkoxy-2,4-dimethylpent-2-enyl)tributylstannanes and aldehydes

E. J. Thomas, A. Teerawutgulrag, 1993 .

On the use of E-1-methoxymethoxybut-2-enyl(tri-n-butyl)stannane as a threo-selective, homo-enolate equivalent

E. J. Thomas, A. Pratt, 1982 .

1,9-Stereocontrol from 1,7-induction using an allylstannane followed by an Ireland-Claisen rearrangement

E. J. Thomas, Ella-Maria Moffatt, E. Thomas, 1999 .

1,4-Asymmetric induction in reactions between [2-(1-alkoxyalkyl)propenyl](tributyl)stannanes and aldehydes promoted by tin(IV) halides

E. J. Thomas, M. Gruttadauria, 1995 .

Synthesis of α-substituted allyl- and homoallyl-stannanes by selenoxide elimination

E. J. Thomas, V. J. Jephcote, E. Thomas, 1991 .

Further studies of an approach to a total synthesis of phomactins

E. J. Thomas, M. Helliwell, Alan T. L. Lee, 2009 .

Approaches to the total synthesis of phomactins

E. J. Thomas, P. Shapland, Graham McGowan, 2003 .

Synthetic approaches to phomactins: Late stage stereochemical and reactivity issues

E. J. Thomas, E. Burnell, Alan T. L. Lee, 2018, Tetrahedron.

Synthetic approaches to phomactins: Novel oxidation of homoallylic alcohols using tetra-n-propylammonium perruthenate

E. J. Thomas, T. Blackburn, 2018, Tetrahedron.

Synthetic approaches to phomactins: on the stereoselectivity of some [2,3]-Wittig rearrangements

E. J. Thomas, T. Blackburn, Michael J. Kilner, 2015 .

Approaches to phomactin A: unexpected late-stage observations

E. J. Thomas, E. Burnell, J. Raftery, 2015 .

Synthesis of precursors of phomactins using [2,3]-Wittig rearrangements

E. J. Thomas, P. Shapland, 2009 .

Stereoselective synthesis of cis- and trans-2,6-disubstituted 5,6-dihydro-2H-pyrans based on 1,5-asymmetric induction in reactions between allylstannanes and aldehydes promoted by tin(IV) chloride

E. J. Thomas, R. Maguire, 1995 .

1,5-Asymmetric induction in reactions between aldehydes and [(4S)-5-(tert-butyldimethylsilyloxy)-4-hydroxypent-2-enyl](tributyl)-stannane promoted by tin(IV) chloride

E. J. Thomas, R. Maguire, 1995 .

Synthesis of macrocyclic precursors of phomactins using [2,3]-Wittig rearrangements.

E. J. Thomas, Graham McGowan, 2009, Organic & biomolecular chemistry.

An approach to an asymmetric synthesis of stemofoline

E. J. Thomas, Clare Vickers, 2009 .

Synthetic approaches to the polycyclic alkaloid stemofoline.

E. J. Thomas, Alison M. Baylis, Michael. P. H. Davies, 2007, Organic & biomolecular chemistry.

Synthesis of the tricyclic nucleus of the alkaloid stemofoline: X-ray crystal structure of (4RS,5RS,7SR,10RS)-10-butyl-5-hydroxy-1-azatricyclo[5.3.0.0]decan-2-one

E. J. Thomas, R. L. Beddoes, Michael. P. H. Davies, 1992 .

An asymmetric synthesis of the pentacyclic core of stemofoline

E. J. Thomas, M. Helliwell, Thomas Burns, 2013 .

A stereoselective synthesis of the C(1)–C(16) fragment of the bryostatins

E. J. Thomas, B. Bradshaw, A. Baron, 2004 .

Asymmetric α-amino acid synthesis: synthesis of (+)-polyoxamic acid using a [3,3]allylic trifluoroacetimidate rearrangement

E. J. Thomas, Ian Savage, 1989 .

Development of a synthesis of lankacidins: stereoselective synthesis of the δ-lactone fragment

E. J. Thomas, Andrew C. Williams, 1995 .

A stereoselective approach to the δ-lactone fragment of the lankacidin antibiotics

E. J. Thomas, Andrew C. Williams, 1987 .

An approach to the total synthesis of lankacidins: synthesis of the requisite building blocks

E. J. Thomas, A. Nelson, Anqi Chen, 2001 .

An approach to the total synthesis of lankacidins: synthesis of advanced macrocyclic precursors

E. J. Thomas, A. Nelson, Anqi Chen, 2001 .

Development and applications of remote stereocontrol using allylic organobismuth reagents.

E. J. Thomas, N. Basar, H. Sirat, 2013, Organic & biomolecular chemistry.

Total synthesis of milbemycin E: synthesis of the C(11)–C(25)fragment

E. J. Thomas, P. Steel, 1997 .

A total synthesis of milbemycin G: approaches to the C1-C10-fragment and completion of the synthesis.

E. J. Thomas, M. Helliwell, Simon R. Bailey, 2005, Organic & biomolecular chemistry.

Total synthesis of milbemycins: a synthesis of (6R)-6-hydroxy-3,4-dihydromilbemycin E.

E. J. Thomas, M. Helliwell, E. Parmee, 2005, Organic & biomolecular chemistry.

Total synthesis of milbemycin G: synthesis of the C(1)–C(10) fragment

E. J. Thomas, Simon R. Bailey, A. Teerawutgulrag, 1995 .

Tricyclic products from the reaction between penicillin derived thiazoloazetidinones and ethyl diazoacetate. X-Ray structure of methyl 2-[(1R, 3S, 4R, 5S, 6S, 8R)-3-benzyl-4,5-bismethoxycarbonyl-6-ethoxycarbonyl-9-oxo-7,10-diaza-2-thiatricyclo[6.2.0.03,7]decan-10-yl]-3-methylbut-2-enoate

David J. Williams, E. J. Thomas, O. Singh, 1982 .

Preparation of 6α-monosubstituted and 6,6-disubstituted penicillanates from 6-diazopenicillanates: reactions of 6-diazopenicillanates with alcohols, thiols, phenylseleninyl compounds, and allylic sulphides, and their analogues

David J. Williams, E. J. Thomas, D. John, 1982 .

Reactions of 6-diazopenicillanates with allylic sulphides, selenides, and bromides

E. J. Thomas, P. Giddings, John Ivor, 1980 .

Synthesis of chiral organotin reagents: synthesis and X-ray crystal structures of bicyclo[2.2.1]heptan-2-yl(diphenyl)tin chlorides with cis-disposed nitrogen containing substituents

E. J. Thomas, D. C. Deka, M. Helliwell, 2001 .

A convergent synthesis of the C(11)–C(25) fragment of the aglycone of avermectin A2b

E. J. Thomas, E. Merifield, M. Smallridge, 1997 .

Milbemycin synthesis: synthesis of a macrocyclic analogue of non-aromatic β-milbemycins

E. J. Thomas, M. Hughes, 1993 .

Milbemycin synthesis: asymmetric synthesis of spiroketals from methyl α-D-glucopyranoside

Nicholas A. Stacey, E. J. Thomas, G. Khandekar, 1993 .

A total synthesis of milbemycin E

E. J. Thomas, P. Steel, E. Parmee, 1989 .

Total synthesis of cytochalasin D: total synthesis and full structural assignment of cytochalasin O

E. J. Thomas, E. Merifield, 1999 .

Cytochalasan synthesis: an alternative approach to cytochalasin D

E. J. Thomas, R. Sauter, J. Watts, 1986 .

Cytochalasan synthesis: Total synthesis of cytochalasin H.

E. J. Thomas, H. Dyke, P. Steel, 1986 .

The Cope Elimination, Sulfoxide Elimination and Related Thermal Reactions

E. J. Thomas, S. Mortlock, P. Astles, 1991 .

Effective 1,7-asymmetric induction in reactions between 6-hydroxyallylstannanes and aldehydes promoted by tin(IV) bromide

E. J. Thomas, J. S. Carey, 1994 .

Asymmetric synthesis of 5,5-disubstituted thiotetronic acids using anallyl xanthate to dithiocarbonate rearrangement: total synthesis of(5S)-thiolactomycin with revision of the absolute configurationof the natural

E. J. Thomas, M. Chambers, E. Thomas, 1997 .

Regioselectivity of selenoxide elimination: synthesis of the cyclohexenediol fragment of non-aromatic β-milbemycins

Nicholas A. Stacey, E. J. Thomas, S. Mortlock, 1987 .

Cytochalasan synthesis: macrocycle formation via intramolecular Diels-Alder reactions

E. J. Thomas, 1991 .

The rearrangement of cyclopropyl chlorides to allyl chlorides

E. J. Thomas, I. Fleming, E. Thomas, 1972 .

The rearrangement of cyclopropyl chlorides to allyl chlorides: stereospecificity in the recapture of the chloride ion

E. J. Thomas, I. Fleming, E. Thomas, 1971 .

Open-chain remote stereocontrol using allylgermanes

E. J. Thomas, Anna P. Weston, 2014 .

1,5-Stereocontrol in reactions of 2,4-disubstituted alk-2-enylstannanes with aldehydes; an approach to the stereoselective synthesis of branched triols

E. J. Thomas, Daniel R. Tray, E. Thomas, 2019 .

Total syntheses of pamamycin 607 and methyl nonactate: stereoselective cyclisation of homoallylic alcohols that had been prepared with remote stereocontrol using allylstannanes.

E. J. Thomas, O. Germay, C. Moore, 2012, Organic & biomolecular chemistry.

An asymmetric synthesis of thiotetronic acids using chirality transfer via an allyl xanthate-to-dithiocarbonate rearrangement. X-Ray crystal structure of (5R)-2,5-dihydro-4-hydroxy-5-methyl-3-phenyl-5-prop-1′-enyl-2-oxothiophene

David J. Williams, E. J. Thomas, M. Chambers, 1987 .

Stereoselective Synthesis of cis-2,5-Disubstituted Tetrahydrofurans: An Approach to Pamamycins

E. J. Thomas, M. Gruttadauria, L. Arista, 1997 .

A preliminary evaluation of a metathesis approach to bryostatins

E. J. Thomas, Raphael Dumeunier, B. Bradshaw, 2006 .

Stereoselective Synthesis of 2-(1-Alkoxyalkyl)-3-hydroxy-5-substituted-tetrahydrofurans

E. J. Thomas, G. Bradley, 1997 .

Total synthesis of a cuticular hydrocarbon from the cane beetle Antitrogus parvulus: confirmation of the relative stereochemistry.

E. J. Thomas, G. Morris, D. Negi, 2012, Organic & biomolecular chemistry.

Synthesis of a 6-aryloxymethyl-5-hydroxy-2,3,4,5-tetrahydro-[1H]-2-benzazepin-4-one: a muscarinic (M3) antagonist.

E. J. Thomas, P. Evans, Alan T. L. Lee, 2008, Organic & biomolecular chemistry.

Approaches to the total synthesis of chaetochalasin A.

E. J. Thomas, Mark Willis, 2014, Organic & biomolecular chemistry.

Cytochalasan synthesis: total synthesis of the naturally occurring [13]cytochalasan proxiphomin

E. J. Thomas, J. Whitehead, 1989 .

The synthesis of a series of adenosine A3 receptor agonists.

E. J. Thomas, E. Burnell, Alan T. L. Lee, 2016, Organic & biomolecular chemistry.

Approaches to cytochalasan synthesis: preparation and Diels–Alder reactions of 3-alkyl- and 3-acyl-Δ3-pyrrolin-2-ones

E. J. Thomas, O. Singh, S. A. Harkin, 1984 .

An approach to the C(17)–C(24) fragment of bryostatins: applications of stereoselective trisubstituted alkene formation by palladium(0) catalysed coupling of enol acetates and vinylic bromides

E. J. Thomas, J. Gràcia, E. Thomas, 1998 .

Total Synthesis of Pamamycin 607: Applications of Remote Asymmetric Induction in Organic Synthesis.

E. J. Thomas, N. Kumar, 2001 .

Synthesis of thiospiroacetals. X-Ray crystal structure determinations for (7RS,11RS)-1,4,8-trioxa-13-thiadispiro[4.1.5.3]pentadecan-11-ol and (4RS,6SR)-4-p-nitrobenzoyloxy-1,7-dithiaspiro[5.5]undecane

E. J. Thomas, M. Helliwell, M. Briggs, 1992 .

Stereoselective synthesis of 4-alkoxy-3-methylidenealkanols usingreactions between 2-(1-alkoxyalkyl)propenylstannanes and aldehydes:X-ray crystal structure of(1R,4R)-3-methylidene-1-(4-nitrophenyl)pentane-1,4-diol

E. J. Thomas, M. Gruttadauria, M. Helliwell, 1997 .

Aspects of remote asymmetric induction using allylstannanes

E. J. Thomas, J. S. Carey, R. Maguire, 1996 .

Remote Asymmetric Induction in Reactions between Allylstannanes and Aldehydes: Influence of a Homoallyl Ether Substituent in the Stannane

E. J. Thomas, J. S. Carey, 1992 .

Chelation controlled reactions between hydroxy- and alkoxy-ketones and prop-2-enyltin trihalides

E. J. Thomas, D. Hallett, 1994 .

1,5-Induction in reactions between 2-alkoxy-(2-tributylstannylethylidene)cyclohexanes and aldehydes

E. J. Thomas, Poonam C. Kumar, Daniel R. Tray, 2001 .

An Observation of Diastereoface Selectivity in Thermal Reactions Between δ-Alkoxyallylstannanes and Aldehydes.

E. J. Thomas, S. Mortlock, 1988 .

Stereoselective Synthesis of Z-Alkenes (III) from α-Methylcrotylstannanes (II) and Aldehydes (I).

E. J. Thomas, S. Mortlock, C. Hull, 1988 .

Stereoselectivity of Reactions Between α-Methylbut-2-enylstannanes and Aldehydes.

E. J. Thomas, S. Mortlock, C. Hull, 1989 .

Aspects of the chemistry of 4-tributylstannyl-, 4-trimethylsilyl- and 2-phenylsulfinylallylstannanes

E. J. Thomas, S. Mortlock, 1998 .

1,5-Asymmetric Induction in Reactions of δ-Alkoxyallylstannanes: Stereoselective Reactions with Chiral Aldehydes.

E. J. Thomas, A. Mcneill, 2010 .

1,5-INDUCTION IN REACTIONS OF 4-ALKOXY-2-TRIMETHYLSILYLALK-2-ENYL(TRIBUTYL)STANNANES WITH ALDEHYDES

E. J. Thomas, Nicholas H. Taylor, 1999 .

ON THE STEREOSELECTIVITY OF REACTIONS OF ALKOXYALLYLSTANNANES AND ALKOXY ALDEHYDES

E. J. Thomas, P. Almendros, 1997 .

Synthesis of cytochalasans using intramolecular Diels–Alder reactions: an alternative approach to cytochalasin D

E. J. Thomas, J. Watts, 1999 .

Stereoselective preparation of 6β -substituted penicillanates

E. J. Thomas, N. Tyrrell, D. John, 1983 .

Triorganotin hydride reduction of 6β-isothiocyanatopenicillanates: a radical-induced sulphur–C(2) bond cleavage

E. J. Thomas, N. Tyrrell, D. John, 1981 .

Preparation and reduction of 6-phenylselenylpenicillanates. A stereoselective synthesis of 6β-substituted penicillanates

E. J. Thomas, P. Giddings, D. IvorJohn, 1980 .

Reduction of 6α-alkyl-6β-isocyanopenicillanates by tri-n-butyltin hydride. A stereoselective synthesis of 6β-alkylpenicillanates

E. J. Thomas, N. Tyrrell, D. John, 1979 .

Preparation and reduction of 6-phenylselenylpenicillanates. A stereoselective synthesis of 6β-substituted penicillanates

E. J. Thomas, P. Giddings, D. IvorJohn, 1980 .

ASPECTS OF NITRILE OXIDE CYCLOADDITION STEREOSELECTIVITY: CHEMISTRY OF 4-CYANO-2,2-DIMETHYL- AND 4-CYANO-2,2,5,5-TETRAMETHYL-1,3-DIOXOLANE OXIDES. X-RAY STRUCTURE OF (4RS, 5RS)-4,5-BIS(METHOXYCARBONYL)-3-((4RS)-2,2,5,5-TETRAMETHYL-1,3

E. J. Thomas, Richard H. Jones, G. C. Robinson, 1984 .

Synthesis of analogues of nucleotides with all-carbon backbones: synthesis of N-protected C-linked dinucleotides

E. J. Thomas, K. Butterfield, 1998 .

An approach to the synthesis of the C(17)–C(27) fragment of bryostatins

E. J. Thomas, E. G. Mata, J. Baxter, 1998 .

An approach to cytochalasan synthesis: macrolide formation by an intramolecular Diels-Alder reaction. X-Ray structure of methyl (1RS, 2SR, 5RS, 6RS)-2,5-dimethyl-1-hydroxy-6-[(1RS)-1-hydroxy-2-phenylethyl]cyclohex-3-ene-1-carboxylate

E. J. Thomas, J. Wallis, S. Vather, 1983 .

Synthesis of antagonists of muscarinic (M3) receptors

E. J. Thomas, Peter E. Penson, Alan T. L. Lee, 2011 .

Fused five-membered hetarenes with one heteroatom

Michael Shipman, J. A. Joule, P. T. Gallagher, 2001 .

Stereoselective synthesis of thymine polyoxin C using an allylic trifluoroacetimidate–trifluoroacetamide rearrangement

E. J. Thomas, P. D. Wilson, Anqi Chen, 1999 .

Stereoselective Synthesis of Thymine Polyoxin C Using an Allylic Trifluoroacetimidate—Trifluoroacetamide Rearrangement.

E. J. Thomas, P. D. Wilson, Anqi Chen, 2000 .

Synthesis of 5-hydroxy-1,7-dioxaspiro[5.5]undec-3-en-2-ones from 2-benzenesulfonyltetrahydropyrans and 5-hydroxybutenolides: X-ray crystal structure determination for (5RS,6SR)-5-acetoxy-4-methoxy3-methyl-1,7-dioxaspiro[5.5]undec-3-en-2-one

E. J. Thomas, M. Helliwell, A. Regan, 1993 .

Stereoselectivity of epoxidation of substituted cyclohexa-1,4-dienes: influence of an allylic methoxycarbonyl group

E. J. Thomas, H. Sirat, T. Mah, 1979 .

Aspects of the chemistry of methyl 3-hydroxycyclohexa-1,5-diene-1-carboxylate: a methyl benzoate hydrate

E. J. Thomas, H. Sirat, N. Tyrrell, 1979 .

Synthesis of 5-Hydroxy-1,7-dioxaspiro(5.5)undec-3-en-2-ones from 2- Benzenesulfonyltetrahydropyrans and 5-Hydroxybutenolides: X-Ray Crystal Structure Determination for (5RS,6SR)-5-Acetoxy-4-methoxy-3- methyl-1,7-dioxaspiro(5.5)undec-3-en-2-one.

E. J. Thomas, M. Helliwell, A. Regan, 1993 .

Total synthesis of milbemycin E: resolution of the C(1)–C(10)fragment and final assembly

E. J. Thomas, P. Steel, E. Parmee, 1997 .

Synthesis of the C(17)-C(27) fragment of the 20-deoxybryostatins

E. J. Thomas, P. Almendros, A. Rae, 2000 .

Total synthesis of (5S)-thiolactomycin: revision of the absolute configuration of the natural product

E. J. Thomas, M. Chambers, E. Thomas, 1989 .

Total Synthesis of (5S)-Thiolactomycin (I): Revision of the Absolute Configuration of the Natural Product.

E. J. Thomas, M. Chambers, 1989 .

An approach to cytochalasin D; 11-membered ring formation using an intramolecular Diels–Alder reaction

E. J. Thomas, A. Craven, D. Tapolczay, 1985 .

Synthesis of C16–C27-fragments of bryostatins modified by 20,20-difluorination

E. J. Thomas, Paul R. Mears, E. Thomas, 2015 .

Synthesis of the C(1)C(16) fragment of bryostatins

E. J. Thomas, M. O’Brien, Nicholas H. Taylor, 2002 .

The stereoselectivity of addition of N-benzyl-C-alkylnitrones to methyl crotonate. X-ray crystal structure of (3RS,4SR,5RS)-2-benzyl-4-methoxy-carbonyl-5-methyl-3-[(4RS)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]isoxazolidine

E. J. Thomas, M. Fray, Richard H. Jones, 1985 .

On the stereoselectivities of some hindered Diels–Alder reactions

E. J. Thomas, J. Raftery, Irem Yalavac, 2015 .

Cytochalasan synthesis: total synthesis of cytochalasin H

E. J. Thomas, J. Whitehead, 1989 .

On the Stereoselectivities of Some Hindered Diels—Alder Reactions.

E. J. Thomas, J. Raftery, Irem Yalavac, 2015 .

Development of a synthesis of lankacidins: an investigation into 17-membered ring formation

E. J. Thomas, E. G. Mata, 1995 .

Development of a Synthesis of Lankacidins: An Investigation into 17- Membered Ring Formation.

E. J. Thomas, E. G. Mata, 1995 .

Cytochalasan syntheses: Synthesis of (17, 18)-17, 18-dihydroxy-10-(prop-2-YL)-14-methyl-[11]cytochalasa-6(7), 13z, 19E-triene-1, 21-dione; an isomer of aspochalasin C

E. J. Thomas, H. Dyke, A. Craven, 1989 .

Cytochalasan Synthesis: Synthesis of (17S,18S)-17,18-Dihydroxy-10-(prop-2-yl)-14-methyl-(11)cytochalasa-6(7),13Z,19E-triene-1,21-dione, an Isomer of Aspochalasin C.

E. J. Thomas, H. Dyke, A. Craven, 1989 .

Aspects of the chemistry of 8-azabicyclo[3.2.1]octanes

E. J. Thomas, Alison M. Baylis, 2007 .

Total synthesis of milbemycin E: development of a procedure for the introduction of the 3,4-double bond and synthesis of the C(1)–C(10) fragment

Nicholas A. Stacey, E. J. Thomas, S. Mortlock, 1997 .

Total Synthesis of Milbemycin E: Development of a Procedure for the Introduction of the 3,4‐Double Bond and Synthesis of the C(1)‐C(10) Fragment.

Nicholas A. Stacey, E. J. Thomas, O. S. Mills, 1997 .

Synthesis of analogues of oligonucleotides; synthesis of unprotected C-linked di- and tri-nucleotides

E. J. Thomas, B. Mellor, 1998 .