P. Bartlett

发表

Crystallographic analysis of transition-state mimics bound to penicillopepsin: phosphorus-containing peptide analogues.

M. James, N. Strynadka, J. Hanson, 1993, Biochemistry.

Chorismate-Utilizing Enzymes Isochorismate Synthase, Anthranilate Synthase, and P-Aminobenzoate Synthase - Mechanistic Insight Through Inhibitor Design

C. Seto, P. Bartlett, M. Kozlowski, 1995 .

A General Method for Molecular Tagging of Encoded Combinatorial Chemistry Libraries

W. C. Still, P. Bartlett, H. Nestler, 1994 .

Purification of 2,5-anhydro-d-hexitol bis(phosphates) and identification of a major 1,4,6-tris(phosphate) contaminant by 31P-, 13C-, and 1H-N.M.R. spectroscopy

P. Bartlett, D. Lankin, R. Voll, 1981 .

Structure-Based Design of an Inhibitor of the Zinc Peptidase Thermolysin

Paul A. Bartlett, Brian W. Matthews, Bradley P. Morgan, 1994 .

Lowering the entropic barrier for binding conformationally flexible inhibitors to enzymes.

M. James, M. Fraser, P. Bartlett, 1998, Biochemistry.

Synthesis of acetylenes from carboxylic acid derivatives via .beta.-keto sulfones

P. Bartlett, F. R. Green, E. Rose, 1978 .

Quantifying amino acid conformational preferences and side-chain-side-chain interactions in beta-hairpins.

Giovanni Piersanti, Scott T Phillips, S. T. Phillips, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Caveat a program to facilitate the structure derived design of biologically active molecules

Paul A. Bartlett, P. Bartlett, G. T. Shea, 1989 .

Exploiting chemical diversity for drug discovery

P. Bartlett, M. Entzeroth, 2006 .

A Template for Stabilization of a Peptide α-Helix: Synthesis and Evaluation of Conformational Effects by Circular Dichroism and NMR

Paul A. Bartlett, Corey W. Liu, D. Wemmer, 1997 .

Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis

P. Bartlett, 1980 .

Synthesis and evaluation of inhibitors of bacterial D-alanine:D-alanine ligases.

P. Bartlett, N. J. Tom, B. Ellsworth, 1996, Chemistry & biology.

Stereochemical course of polymerization catalyzed by avian myeloblastosis virus reverse transcriptase.

P. Bartlett, F. Eckstein, Paul A. BartlettS, 1982, The Journal of biological chemistry.

Macrocyclic Inhibitors of Penicillopepsin. 3. Design, Synthesis, and Evaluation of an Inhibitor Bridged between P2 and P1‘

Paul A. Bartlett, Whitney W. Smith, P. Bartlett, 1998 .

"Phosphate extension". A strategem for the stereoselective functionalization of acyclic homoallylic alcohols

P. Bartlett, K. Jernstedt, 1977 .

Differential Binding Energy: A Detailed Evaluation of the Influence of Hydrogen-Bonding and Hydrophobic Groups on the Inhibition of Thermolysin by Phosphorus-Containing Inhibitors.

J. M. Scholtz, P. Bartlett, M. Ballinger, 1991 .

Potentially Macrocyclic Peptidyl Boronic Acids as Chymotrypsin Inhibitors.

D. P. Mack, P. Bartlett, C. Hutton, 1997, The Journal of organic chemistry.

Inhibition of chymotrypsin by phosphonate and phosphonamidate peptide analogs

P. Bartlett, L. A. Lamden, 1986 .

Novel, Amino Acid-Derived Heterobicycles: Scaffolds for β-Turn Mimics and Targets for Combinatorial Synthesis

P. Bartlett, Leverett R. Smith, 1998 .

An antibody-catalyzed Claisen rearrangement

P. Schultz, P. Bartlett, J. Jacobs, 1988 .

Synthesis of water-soluble undecagold cluster compounds of potential importance in electron microscopic and other studies of biological systems

P. Bartlett, S. J. Singer, B. Bauer, 1978 .

Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis

P. Bartlett, 1980 .

Sequence-specific crosslinking agents for nucleic acids. Use of 6-bromo-5,5-dimethoxyhexanohydrazide for crosslinking cytidine to guanosine and crosslinking RNA to complementary sequences of DNA.

J. Summerton, P. Bartlett, 1978, Journal of molecular biology.

Design of Enzyme Inhibitors

P. Bartlett, 1996 .

Cyclic hexapeptides and chimeric peptides as mimics of tendamistat

M. Lipton, P. Bartlett, S. Goldberg, 1994 .

Inhibition of EPSP Synthase by Analogues of the Tetrahedral Intermediate and of EPSP.

P. Bartlett, D. Alberg, A. Faessler, 1992 .

Potent inhibition of 5-enolpyruvylshikimate-3-phosphate synthase by a reaction intermediate analogue

P. Bartlett, D. Alberg, 1989 .

The Interplay Between Enzyme Mechanism, Protein Structure, and Inhibitor and Catalyst Design

P. Bartlett, 1988 .

Phosphonamidate inhibitors of human neutrophil collagenase.

H. V. Van Wart, P. Bartlett, K. Mookhtiar, 1987, Biochemistry.

Synthesis and evaluation of inhibitors for Escherichia coli carbamyl phosphate synthetase

J. M. Scholtz, P. Bartlett, 1989 .

Conservation of mechanism in three chorismate-utilizing enzymes.

P. Bartlett, M. Toney, Ze He, 2004, Journal of the American Chemical Society.

Synthetic Design for Combinatorial Chemistry. Solution and Polymer-Supported Synthesis of Polycyclic Lactams by Intramolecular Cyclization of Azomethine Ylides

P. Bartlett, M. Marx, A. Grillot, 1997 .

5 – Olefin Cyclization Processes That Form Carbon–Carbon Bonds

P. Bartlett, 1984 .

Synthesis and evaluation of an inhibitor of carboxypeptidase A with a Ki value in the femtomolar range.

P. Bartlett, A. Kaplan, Paul A. Bartlett, 1991, Biochemistry.

A phosphonamidate dipeptide analog as an inhibitor of carboxypeptidase A

P. Bartlett, N. Jacobsen, 1981 .

Synthesis of .beta.-acylacrylic esters and .alpha.,.beta.-butenolides via .beta.-keto sulfoxide alkylation

P. Bartlett, 1976 .

The Haciendas of Mexico: An Artist's Record

P. Bartlett, 1990 .

Amino acid derived heterocycles: lewis acid catalyzed and radical cyclizations from peptide acetals.

M. Todd, P. Bartlett, Chudi O. Ndubaku, 2002, The Journal of organic chemistry.

Phosphorus amino acid analogues as inhibitors of leucine aminopeptidase.

P. Bartlett, P. Giannousis, 1987, Journal of medicinal chemistry.

MACROCYCLIC INHIBITORS OF PENICILLOPEPSIN. 1. DESIGN, SYNTHESIS, AND EVALUATION OF AN INHIBITOR BRIDGED BETWEEN P1 AND P3

P. Bartlett, J. H. M. and, 1998 .

Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid

P. Bartlett, L. Mcquaid, 1984 .

Approaches to the synthesis of the tetrahydropyran subunit of the polyether nigericin

C. Holmes, P. Bartlett, 1989 .

Stereocontrolled synthesis of trans-2,5-disubstituted tetrahydrofurans

P. Bartlett, P. Ting, 1984 .

Radical cyclization of oxime ethers

P. Bartlett, P. Ting, K. L. Mclaren, 1988 .

Crystal structures of alpha-lytic protease complexes with irreversibly bound phosphonate esters.

D. Agard, R. Bone, N. Sampson, 1993, Biochemistry.

Peptidic phosphonylating agents as irreversible inhibitors of serine proteases and models of the tetrahedral intermediates.

N. Sampson, P. Bartlett, 1991, Biochemistry.

Potent inhibition of pepsin and penicillopepsin by phosphorus-containing peptide analogues

J. Hanson, P. Bartlett, P. Giannousis, 1990 .

A phosphonamidate dipeptide analog as an inhibitor of carboxypeptidase A

P. Bartlett, N. Jacobsen, 1981 .

Binding Energy and Catalysis: The Implications for Transition-State Analogs and Catalytic Antibodies.

Mary M. Mader, Paul A. Bartlett, P. Bartlett, 1997, Chemical reviews.

Synthesis of Two Potential Inhibitors of para-Aminobenzoic Acid Synthase.

P. Bartlett, K. D. Stigers, Roger Mar-Tang, 1999, The Journal of organic chemistry.

OLEFIN CYCLIZATION PROCESSES THAT FORM CARBON‐HETEROATOM BONDS

P. Bartlett, 1985 .

6 – Olefin Cyclization Processes That Form Carbon–Heteroatom Bonds

P. Bartlett, 1984 .

Enantiodivergent syntheses of (+)- and (−)-nonactic acid and the total synthesis of nonactin

James D. Meadows, E. Ottow, P. Bartlett, 1984 .

Chorismate mutase inhibitors: synthesis and evaluation of some potential transition-state analogs

Charles R. Johnson, P. Bartlett, A. Luis, 1988 .

Phosphinic acid dipeptide analogs: potent, slow-binding inhibitors of aspartic peptidases

P. Bartlett, W. B. Kezer, 1984 .

FLUOROALKENES AS PEPTIDE ISOSTERES : GROUND STATE ANALOG INHIBITORS OF THERMOLYSIN

P. Bartlett, A. Otake, 1995 .

OLEFIN CYCLIZATION PROCESSES THAT FORM CARBON-CARBON BONDS

P. Bartlett, 1984 .

Differential binding energy: a detailed evaluation of the influence of hydrogen-bonding and hydrophobic groups on the inhibition of thermolysin by phosphorus-containing inhibitors

Paul A. Bartlett, Bradley P. Morgan, J. M. Scholtz, 1991 .

Synthesis of phosphonic acid derivatives by oxidative activation of phosphinate esters

N. Sampson, P. Bartlett, 1988 .

Carbonate extension. A versatile procedure for functionalization of acyclic homoallylic alcohols with moderate stereocontrol

James D. Meadows, P. Bartlett, A. Morimoto, 1982 .

Phosphonate analogues of carboxypeptidase A substrates are potent transition-state analogue inhibitors.

J. Hanson, P. Bartlett, A. Kaplan, 1989, Biochemistry.

Evaluation of intrinsic binding energy from a hydrogen bonding group in an enzyme inhibitor.

P. Bartlett, C. Marlowe, 1987, Science.

Aminoalkylphosphonofluoridate derivatives: rapid and potentially selective inactivators of serine peptidases.

P. Bartlett, L. A. Lamden, 1983, Biochemical and biophysical research communications.

19 – Interplay among Enzyme Mechanism, Protein Structure, and the Design of Serine Protease Inhibitors

D. Drewry, N. Sampson, P. Bartlett, 1990 .

High diastereofacial selectivity in nucleophilic additions to chiral thionium ions

P. Bartlett, I. Mori, C. Heathcock, 1987 .

Acyclic stereoselection. 52. On the mechanism of Lewis acid mediated nucleophilic substitution reactions of acetals

P. Bartlett, K. Ishihara, I. Mori, 1990 .

Stereoselective additions of nucleophilic alkenes to chiral thionium ions

P. Bartlett, I. Mori, C. Heathcock, 1990 .

Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcohols

J. D. Elliott, P. Bartlett, W. S. Johnson, 1983 .

Diastereoselectivity in the alkylation of chiral 2-aminomethyl-1,3,2-dioxaphosphorinane 2-oxides

P. Bartlett, K. L. Mclaren, 1987 .

β Strand Peptidomimetics as Potent PDZ Domain Ligands

Wendell A. Lim, Paul A. Bartlett, Ming C. Hammond, 2006 .

Brief Communication b Strand Peptidomimetics as Potent PDZ Domain Ligands

W. Lim, P. Bartlett, M. C. Hammond, 2006 .

Cyclic phosphonic-carboxylic imides and anhydrides as reactive intermediates. 1. Rearrangement and solvolysis of N-(amino(methyl)phosphinyl)-L-phenylalanine derivatives

P. Bartlett, N. Jacobsen, 1983 .

PHOSPHINIC ACID DIPEPTIDE ANALOGS: POTENT, SLOW‐BINDING INHIBITORS OF ASPARTIC PEPTIDASES

P. Bartlett, W. B. Kezer, 1984 .

A thioamide substrate of carboxypeptidase A.

P. Bartlett, N. Jacobsen, K. Spear, 1982, Biochemistry.

Synthetic strategies in combinatorial chemistry.

P. Bartlett, M. Spaller, M. Burger, 1997, Current opinion in chemical biology.

Ester-enolate Claisen rearrangement of .alpha.-amino acid derivatives

P. Bartlett, J. Barstow, 1982 .

ENANTIODIVERGENT SYNTHESES OF (+)‐ AND (‐)‐NONACTIC ACID AND THE TOTAL SYNTHESIS OF NONACTIN

James D. Meadows, E. Ottow, P. Bartlett, 1984 .

Stereocontrolled synthesis of cis-2,5-disubstituted tetrahydrofurans and cis- and trans-linalyl oxides

P. Bartlett, S. Rychnovsky, 1981 .

Stereocontrolled synthesis of tetrahydrofurans and tetrahydropyrans using thallium(III)-induced cyclizations

P. Bartlett, J. Michael, P. Ting, 1985 .

Conversion of shikimic acid to 5-enolpyruvylshikimate 3-phosphate

P. Bartlett, Paul M. Chouinard, 1986 .

.alpha.-Diazophosphonic acids as potential photoaffinity labeling reagents: synthesis, stability, and photochemistry

N. Carruthers, P. Bartlett, B. Winter, 1982 .

A new class of potential photoaffinity labels. .alpha.-Diazophosphonic acids: synthesis and stability

P. Bartlett, K. P. Long, 1977 .

Metal Coordination as a Method for Templating Peptide Conformation

Paul A. Bartlett, P. Bartlett, Zong-Qiang Tian, 1996 .

An improved reagent for the o-alkyl cleavage of methyl esters by nucleophilic displacement

P. Bartlett, W. S. Johnson, 1970 .

Stereoselective epoxidation of acyclic olefinic carboxylic acids via iodolactonization

J. Myerson, P. Bartlett, 1978 .

Electrophilic lactonization as a tool in acyclic stereocontrol. Synthesis of serricornin

J. Myerson, P. Bartlett, D. P. Richardson, 1984 .

A stereoselective total synthesis of the Prelog-Djerassi lactone

J. Adams, P. Bartlett, 1980 .

Substrate analogs as mechanistic probes for the bifunctional chorismate synthase from Neurospora crassa.

P. Bartlett, C. T. Lauhon, 1994, Biochemistry.

Synthetic Organic Chemistry and the Shikimate Pathway: Inhibitors and Intermediates

P. Bartlett, 1986 .

Cycloaddition. IV. Addition Products of 1,1-Dichloro-2,2-difluoroethylene to a Further Series of Dienes

P. Bartlett, L. Montgomery, Gunter Wallbillich, 1967 .

Stereocontrolled total synthesis of (.+-.)-tirandamycin A

J. Myerson, P. Bartlett, C. Neukom, 1986 .

Ester-enolate Claisen rearrangement of lactic acid derivatives

P. Bartlett, J. Barstow, D. J. Tanzella, 1982 .

Stereochemical control of the ynamine-Claisen rearrangement

P. Bartlett, W. Hahne, 1979 .

Activation Parameters and Stereochemistry of an Antibody‐Catalyzed Claisen Rearrangement

P. Schultz, P. Bartlett, D. Y. Jackson, 1992 .

Preparation and reactions of an alkylzinc enolate

P. Bartlett, M. M. Hansen, C. Heathcock, 1987 .

Stereoselective synthesis of the dihydroxyisoleucine constituent of the amanita mushroom toxins

P. Bartlett, J. Barstow, D. J. Tanzella, 1982 .

Evaluation of the Claisen rearrangement of 2-cyclohexenols for the stereoselective construction of a terpene synthon

P. Bartlett, C. Pizzo, 1981 .

Stereochemical control of the ynamine-Claisen rearrangement

P. Bartlett, W. Hahne, 1979 .

A mild, oxidative nitro-to-carbonyl conversion and a new prostaglandin synthon

T. Webb, P. Bartlett, F. R. Green, 1977 .

A stereospecific total synthesis of estrone via a cationic olefinic cyclization.

P. Bartlett, W. S. Johnson, 1973, Journal of the American Chemical Society.

Investigation of an octapeptide inhibitor of Escherichia coli ribonucleotide reductase by transferred nuclear Overhauser effect spectroscopy.

J. Bushweller, P. Bartlett, 1991, Biochemistry.

Formation of the 7-Oxa-1,4,10-triazatricyclo[8.2.2(5,12)]tetradecane-2,14-dione Ring System: Misrouted Synthesis of a Peptidomimetic.

P. Bartlett, M. Kozlowski, 1996, The Journal of organic chemistry.

A subtotal synthesis of methynolide via an electrophilic spirocyclization reaction

P. Bartlett, I. Mori, J. Bose, 1989 .

Construction of trans-fused polycyclic ethers: methodology for the brevetoxins

P. Bartlett, P. Ting, 1986 .

Synthesis of polyether-type tetrahydrofurans via hydroperoxide cyclization

P. Bartlett, C. Chapuis, 1986 .

Stereocontrolled synthesis of a polyether fragment

P. Bartlett, A. Morimoto, K. Holm, 1985 .

A stereocontrolled synthesis of the methyl ester of (±)-nonactic acid

P. Bartlett, K. Jernstedt, 1980 .

Electrophilic lactonization as a tool in acyclic stereocontrol. Synthesis of serricornin

J. Myerson, P. Bartlett, D. P. Richardson, 1984 .

Radical Cyclization of Oxime Ethers.

P. Bartlett, P. Ting, K. L. Mclaren, 1988 .

Phosphorus-containing peptide analogs as peptidase inhibitors.

J. Hanson, P. Bartlett, C. Marlowe, 1987, Cold Spring Harbor symposia on quantitative biology.

Inhibition of thermolysin by phosphonamidate transition-state analogues: measurement of 31P-15N bond lengths and chemical shifts in two enzyme-inhibitor complexes by solid-state nuclear magnetic resonance.

T. Oas, R. Griffin, D. Drewry, 1990, Biochemistry.

Cyclic phosphonic-carboxylic imides and anhydrides as reactive intermediates. 2. Solvolysis of N-(hydroxy(methyl)phosphinothioyl)-L-phenylalanine derivatives

P. Bartlett, N. Jacobsen, 1983 .

An α-diazophosphonic acid monoester: synthesis, stability, and unexpected photochemical behaviour

N. Carruthers, P. Bartlett, 1982 .

Phosphorus-containing purines and pyrimidines: A new class of transition state analogs

J. Adams, J. Hunt, P. Bartlett, 1978 .

Phosphonate Inhibitors of Carboxypeptidase A

P. Bartlett, N. Jacobsen, 1981 .

An Analysis of the Enzyme-Inhibitor Binding Interactions for Phosphonic Acid Transition State Analogs of Thermolys in

P. Bartlett, C. Marlowe, 1987 .

Transition State Analogy of Phosphonic Acid Peptide Inhibitors of Pepsin

P. Bartlett, Mark A. Giangiordano, 1996 .

Transition-state characterization: a new approach combining inhibitor analogues and variation in enzyme structure.

W. Rutter, P. Bartlett, M. A. Phillips, 1992, Biochemistry.

Possible role for water dissociation in the slow binding of phosphorus-containing transition-state-analogue inhibitors of thermolysin.

P. Bartlett, C. Marlowe, P A Bartlett, 1987, Biochemistry.

Phosphonamidates as transition-state analogue inhibitors of thermolysin.

P. Bartlett, C. Marlowe, 1983, Biochemistry.

Structural study of the complex between human pepsin and a phosphorus-containing peptidic -transition-state analog.

M. James, M. Fujinaga, N. Tarasova, 2000, Acta crystallographica. Section D, Biological crystallography.

5-enolpyruvylshikimate 3-phosphate synthase: chemical synthesis of the tetrahedral intermediate and assignment of the stereochemical course of the enzymatic reaction.

P. Bartlett, U. Maitra, M. An, 2003, Journal of the American Chemical Society.

CAVEAT: A program to facilitate the design of organic molecules

Paul A. Bartlett, Georges Lauri, P. Bartlett, 1994, J. Comput. Aided Mol. Des..

ENZYMATIC, POLYMER-SUPPORTED FORMATION OF AN ANALOG OF THE TRYPSIN INHIBITOR A90720A : A SCREENING STRATEGY FOR MACROCYCLIC PEPTIDASE INHIBITORS

P. Bartlett, M. Burger, 1997 .

Differential inhibition of class I and class II 5-enolpyruvylshikimate-3-phosphate synthases by tetrahedral reaction intermediate analogues.

M. Healy-Fried, T. Funke, Huijong Han, 2007, Biochemistry.

Enzymatic synthesis of a ring-contracted analogue of 5-enolpyruvylshikimate-3-phosphate.

P. Bartlett, M. An, 2004, Organic letters.

An inhibitor of chorismate mutase resembling the transition-state conformation

Charles R. Johnson, P. Bartlett, 1985 .

“@-Tides”: The 1,2-Dihydro-3(6H)-pyridinone Unit as a β-Strand Mimic

Scott T. Phillips, Paul A. Bartlett, Michael Kossenjans, 2002 .

A disulfide-bridge bifunctional imidoester as a reversible cross-linking reagent.

S. Singer, P. Bartlett, A. Ruoho, 1975, Biochemical and biophysical research communications.

Inhibition of 5-enolpyruvoylshikimate 3-phosphate (EPSP) synthase by analogs of the tetrahedral intermediate and of EPSP

P. Bartlett, D. Alberg, A. Faessler, 1992 .

Design and use of potent, specific enzyme inhibitors.

G. Stark, P. Bartlett, 1983, Pharmacology & therapeutics.

Observation of an undecagold cluster compound in the scanning transmission electron microscope

J. Hainfeld, J. Wall, P. Bartlett, 1982 .

The Total Synthesis of Ipalbidine and Ipalbine

P. Bartlett, D. Dolphin, A. Wick, 1971 .

Does dehydroquinate synthase synthesize dehydroquinate

P. Bartlett, K. Satake, 1988 .

Inhibition of Escherichia coli cytidine deaminase by a phosphapyrimidine nucleoside.

G. Ashley, P. Bartlett, 1984, The Journal of biological chemistry.

Purification and properties of cytidine deaminase from escherichia coli.

G. Ashley, P. Bartlett, 1984, Journal of Biological Chemistry.

Synthesis of (‐)‐2‐Chloroshikimic Acid

P. Bartlett, B. M. Lawrence, R. H. Rich, 1994 .

Synthesis of "iso-EPSP" and evaluation of its interaction with chorismate synthase

P. Bartlett, U. Maitra, Paul M. Chouinard, 1986 .

Synthesis of (-)-2-chloroshikimic acid

P. Bartlett, B. M. Lawrence, R. H. Rich, 1994 .

Synthesis of “Iso-EPSP” and Evaluation of Its Interaction with Chorismate Synthase.

P. Bartlett, U. Maitra, Paul M. Chouinard, 1987 .

Preparation of diazabicyclo[4.3.0]nonene-based peptidomimetics.

P. Bartlett, C. Hutton, 2007, The Journal of organic chemistry.

Attempted De Novo design, synthesis, and evaluation of a ligand for the allosteric site of phosphofructokinase

N. Sampson, P. Bartlett, 1991 .

Crystal structure determination, refinement and molecular model of creatine amidinohydrolase from Pseudomonas putida.

R. Huber, P. Bartlett, S. Knof, 1988, Journal of molecular biology.

STEREOCONTROL VIA CYCLIZATION REACTIONS

P. Bartlett, 1983 .

A convenient differential protection strategy for functional group manipulation of aspartic and glutamic acids

J. M. Scholtz, P. Bartlett, 1989 .

Combinatorial synthetic design. Solution and polymer-supported synthesis of heterocycles via intramolecular aza Diels-Alder and imino alcohol cyclizations.

P. Brennan, P. Bartlett, M. Spaller, 2002, Journal of combinatorial chemistry.

In Silico Surrogates for In Vivo Properties: Profiling for ADME and Toxicological Behavior

P. Bartlett, M. Entzeroth, 2006 .

Total synthesis of brefeldin A

P. Bartlett, F. R. Green, 1978 .

A highly stereoselective synthesis of davanone

C. Holmes, P. Bartlett, 1983 .

Synthesis of (-)-2-Fluoroshikimic Acid.

P. Bartlett, R. H. Rich, 1996, The Journal of organic chemistry.

Synthesis of (‐)‐2‐Fluoroshikimic Acid.

P. Bartlett, R. H. Rich, 1996 .

The Use of Polymer-Assisted Solution-Phase Synthesis and Automation for the High-Throughput Preparation of Biologically Active Compounds

P. Bartlett, M. Entzeroth, 2006 .

Synthesis of amino acid-derived cyclic acyl amidines for use in beta-strand peptidomimetics.

P. Bartlett, M. C. Hammond, 2007, The Journal of organic chemistry.

Facile synthesis of @-tide beta-strand peptidomimetics: improved assembly in solution and on solid phase.

S. T. Phillips, P. Bartlett, Bettina van Lengerich, 2004, Organic letters.

An improved synthesis of the transition state analog inhibitor of chorismate mutase

Whitney W. Smith, P. Bartlett, 1993 .

An Inhibitor of Chorismate Mutase Resembling the Transition-State Conformation.

Charles R. Johnson, P. Bartlett, 1986 .

Stereoselective synthesis of 2-(2′-cycloalkenyl)glycinates via ester-enolate claisen rearrangement

P. Bartlett, J. Barstow, 1982 .

Beta strand peptidomimetics as potent PDZ domain ligands.

Wendell A Lim, W. Lim, P. Bartlett, 2006, Chemistry & biology.

Interaction of phosphonate analogues of the tetrahedral reaction intermediate with 5-enolpyruvylshikimate-3-phosphate synthase in atomic detail.

Gerald H Lushington, Ernst Schönbrunn, A. Becker, 2005, Biochemistry.

Synthesis and Evaluation of Macrocyclic Transition State Analogue Inhibitors for α-Chymotrypsin

P. Bartlett, Kristina K. Hansen, B. Grosch, 2003 .

Macrocyclic Inhibitors of Penicillopepsin. 2. X-ray Crystallographic Analyses of Penicillopepsin Complexed with a P3−P1 Macrocyclic Peptidyl Inhibitor and with Its Two Acyclic Analogues

M. James, M. Fraser, P. Bartlett, 1998 .

Crystallographic analysis of transition-state mimics bound to penicillopepsin: phosphorus-containing peptide analogues.

M. James, N. Strynadka, J. Hanson, 1993, Biochemistry.