Synthesis of (2R)- and (2S)-[1-13C]-2-amino-2-methylmalonic acid, probes for the serine hydroxymethyltransferase reaction: stereospecific decarboxylation of the 2-pro-R carboxy group with the retention of configuration-Reference-Cited by-同舟云学术

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Synthesis of (2R)- and (2S)-[1-13C]-2-amino-2-methylmalonic acid, probes for the serine hydroxymethyltransferase reaction: stereospecific decarboxylation of the 2-pro-R carboxy group with the retention of configuration

Published:1990 Issue:5 Volume: Page:400
ISSN:0022-4936
Container-title:Journal of the Chemical Society, Chemical Communications
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Thomas Neil R.,Schirch Verne,Gani David

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1990/C3/C39900000400

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Revealing protonation states and tracking substrate in serine hydroxymethyltransferase with room-temperature X-ray and neutron crystallography;Communications Chemistry;2023-08-03

2. Enantioselective Synthesis of Chiral α-Azido and α-Aryloxy Quaternary Stereogenic Centers via the Phase-Transfer-Catalyzed α-Alkylation of α-Bromomalonates, Followed by SN2 Substitution;The Journal of Organic Chemistry;2017-04-20

3. Construction of Chiral α-Amino Quaternary Stereogenic Centers via Phase-Transfer Catalyzed Enantioselective α-Alkylation of α-Amidomalonates;The Journal of Organic Chemistry;2015-02-26

4. Alkylation and Related Reactions IV;Key Chiral Auxiliary Applications;2014

5. 7.19 C–X Bond Formation: Enzymatic Enantioselective Decarboxylative Protonation and C–C Bond Formation;Comprehensive Chirality;2012

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