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Dive into the research topics where Jeffrey A. Coderre is active.

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Featured researches published by Jeffrey A. Coderre.


Tetrahedron Letters | 1980

Syntheses and configurational assignments of the diastereomers of the 4-nitrophenyl esters of thymidine 3′-(N-phenyl phosphoramidate) and thymidine 5′-(N-phenyl phosphoramidate)

John A. Gerlt; Shujaath Mehdi; Jeffrey A. Coderre; William O. Rogers

Abstract The separated diastereomers of 3′-(4-nitrophenyl N-phenyl phosphoramidate)-5′-monomethoxytrityl thymidine and 3′-monomethoxytrityl-5′-(4-nitrophenyl N-phenyl phosphoramidate) thymidine have been prepared and their absolute configurations at phosphorus have been determined.


Journal of the American Chemical Society | 1981

Oxygen chiral phosphodiesters. 4. Stereochemical course of the hydrolysis of 2'-deoxyadenosine cyclic 3',5'-[17O, 18O]monophosphate in water(oxygen-16) catalyzed by bovine heart cyclic nucleotide phosphodiesterase

Jeffrey A. Coderre; Shujaath Mehdi; John A. Gerlt


Journal of the American Chemical Society | 1980

Oxygen chiral phosphodiesters. 1. Synthesis and configurational analysis of cyclic [18O]-2′-deoxyadenosine 3′,5′-monophosphate [11]

John A. Gerlt; Jeffrey A. Coderre


Journal of the American Chemical Society | 1980

Oxygen chiral phosphodiesters. 2. Enzymatic synthesis and configurational analysis of [α-18O]-2′-deoxyadenosine 5′-diphosphate [27]

Jeffrey A. Coderre; John A. Gerlt


Advances in Enzymology and Related Areas of Molecular Biology | 1983

Oxygen Chiral Phosphate Esters

John A. Gerlt; Jeffrey A. Coderre; Shujaath Mehdi


Journal of the American Chemical Society | 1981

Oxygen chiral phosphodiesters. 3. Use of 17O NMR spectroscopy to demonstrate configurational differences in the diastereomers of cyclic 2′-deoxyadenosine 3′,5′-[17O,18O]monophosphate

Jeffrey A. Coderre; Shujaath Mehdi; Peter C. Demou; Richard Weber; Daniel D. Traficante; John A. Gerlt


Tetrahedron | 1983

Oxygen chiral phosphodiesters-8. Stereochemical course of the base-catalyzed hydrolysis of cyclic 2'-deoxyadenosine 3',5'-[17O, 18O]monophosphate

Shujaath Mehdi; Jeffrey A. Coderre; John A. Gerlt


Archive | 2011

Mechanism of the Adenylate Cyclase Reaction

Brevibacterium Liquefaciens; John A. Gerlt; Jeffrey A. Coderre; S Michael


Archive | 1981

Syntheses and Configurational Assignments of Thymidine 3′- and 5′-(4-Nitrophenyl [17O,18O] Phosphates)

Shujaath Mehdi; Jeffrey A. Coderre; John A. Gerlt


ChemInform | 1981

OXYGEN CHIRAL PHOSPHODIESTERS. 4. STEREOCHEMICAL COURSE OF THE HYDROLYSIS OF 2′-DEOXYADENOSINE CYCLIC 3′,5′-(17O, 18O)MONOPHOSPHATE IN WATER(OXYGEN-16) CATALYZED BY BOVINE HEART CYCLIC NUCLEOTIDE PHOSPHODIESTERASE

Jeffrey A. Coderre; Shujaath Mehdi; John A. Gerlt

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