13C NMR Evidence for an Enzyme-Induced Lossen Rearrangement in the Mechanism-Based Inactivation of α-Chymotrypsin by 3-Benzyl-N-((methylsulfonyl)oxy)succinimide

DOI: 10.1021/ja00187a086

Source and publish data:

Journal of the American Chemical Society p. 1931 - 1932 (1989)

Update date:2022-07-30

Topics:

Authors:

Groutas, William C.

Stanga, Michael A.

Brubaker, Michael J.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja00187a086

Full text of DOI:10.1021/ja00187a086

Products guided by the article

Product name:C₁₀⁽¹³⁾CH₁₂O₄

Cas No:119880-91-0

R&D Labs maybe for 119880-91-0

Shanghai Egoal Chemical Co.,Ltd

Contact:+86-21-50333091

Address:Yangming Garden Square 3,YangGao North Road 1188, Pudong New District, Shanghai
Zhengzhou HQ Material Co.,Ltd

Contact:+86-371-67759225

Address:No.32, Jinsuo Road, High-tech Zone
MTT Pharma & Bio-technology Co.,Ltd(expird)

Contact:+86-21-58407925

Address:Room2019, Building C, Tomson Center, No.158, Zhang Yang Road, Shanghai, China
JIN TAN CHENG'EN CHEMICAL CO.,LTD.

Contact:86-519-82116250

Address:NO.102，village Dongfang，conomic development zone
Luna Chemicals Co.,Ltd.

Contact:+86-570-4336358

Address:No.87 Building,Tianqian,Sidu Town

Relevant to this article

Discovery of potent IDO1 inhibitors derived from tryptophan using scaffold-hopping and structure-based design approaches

Doi:10.1016/j.ejmech.2017.06.039
(2017)
PHOTOSTIMULATED REACTIONS OF HALOARENES WITH 2-NAPHTHYLAMIDE IONS. A FACILE SYNTHESIS OF 1-ARYL-2-NAPHTHYLAMINES.

Doi:10.1016/S0040-4039(00)96588-2
(1987)
A facile preparation of α-aryl carboxylic acid via one-flow arndt-eistert synthesis

Doi:10.1071/CH15342
(2015)
Stereochemistry of benzylic carbon substitution coupled with ring modification of 2-nitrobenzyl groups as key determinants for fast-cleaving reversible terminators

Doi:10.1002/anie.201106516
(2012)
Synthesis of n-(3-cyano-7-ethoxy-1,4-dihydro-4-oxoquinolin-6-yl)acetamide

Doi:10.3987/COM-11-12343
(2011)
Structure activity optimization of 6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazines as Jak1 kinase inhibitors

Doi:10.1016/j.bmcl.2015.09.020
(2015)

Article Doi