Synthesis of (2R)- and (2S)- [1-13C]-2-amino-2-methylmalonic acid: Chiral substrates for serine hydroxymethyltransferase

Tetrahedron

Volumn 47, Issue 3, 1991, Pages 497-506

  Thomas, Neil R ^a   Gani, David ^a  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CARBON 13; TRANSFERASE;

ARTICLE; ENZYME MECHANISM; REACTION ANALYSIS;

EID: 0026098623     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)90505-8     Document Type: Article

References (20)

1. Enantioselective Synthesis ofα-Methylserines
2. Enantioselective synthesis of (R)- and (S)-4-methylcycloserine by the bislactim ether method
3. Asymmetrische Synthese von α-Methylaminosäure-methylestern unter Verwendung von D-Galactodialdehydals chiralem Hilfsreagens
4. Enantioselective Syntheses of(R)-Amino Acids UsingL-Valine as Chiral Agent
5. A NOVEL SYNTHESIS OF N-CARBOXY-α-AMINO ACID ANHYDRIDE
6. Asymmetric syntheses via heterocyclic intermediates, XL. Studies on the acylation of lithiated bislactim ethers of cyclo(-L-Val-Ala-) and cyclo(-L-Val-Gly-) Asymmetric synthesis of (R)-α-alkenyl and (R)-α-ethinyl alanine methyl esters by the bislactim ether method
7. 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