A stereoselective oxy-Michael route to protected β-aryl-β- hydroxy-α-amino acids

Synlett

Volumn , Issue 16, 2006, Pages 2673-2675

  Hernandez Juan, Felix A ^a   Richardson, Robert D ^a   Dixon, Darren J ^b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

hydroxy amino acids; (S) 6 methyl tetrahydropyran 2 ol; oxy Michael addition; Stereoselectivity

Indexed keywords

6 METHYL TETRAHYDROPYRAN 2 OL; AMINO ACID DERIVATIVE; BETA ARYL BETA HYDROXY ALPHA AMINO ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; MICHAEL ADDITION; STEREOCHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 33750036430     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-950434     Document Type: Article

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