Highly enantioselective synthesis of orthogonally protected (2S)-2,3-diaminopropanoates through catalytic phase-transfer aza-Henry reaction

Helvetica Chimica Acta

Volumn 94, Issue 8, 2011, Pages 1543-1550

  Kumaraswamy, Gullapalli ^a   Pitchaiah, Arigala ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

, Diamino acids; (2S) Propanoic acids, 2,3 diamino ; Aza Henry reaction; Catalysis; Cinchona alkaloid; Glycosidase inhibitors; Inhibitors; Organocatalysis

Indexed keywords

AZA-HENRY REACTION; CINCHONA ALKALOID; DIAMINO ACIDS; GLYCOSIDASE INHIBITORS; ORGANOCATALYSIS; PROPANOIC ACID;

AMINO ACIDS; CARBONYLATION; CATALYSIS; CHIRALITY; ENANTIOMERS; ENANTIOSELECTIVITY; RATE CONSTANTS; REACTION KINETICS; STEREOCHEMISTRY;

SYNTHESIS (CHEMICAL);

METHYL 2 [[(BENZYLOXY)CARBONYL]AMINO] 3 [[(9H FLUOREN 9 YLMETHOXY)CARBONYL]AMINO]PROPANOATE; METHYL 2 [[(BENZYLOXY)CARBONYL]AMINO] 3 [[(TERT BUTOXY)CARBONYL]AMINO]PROPANOATE; METHYL 2 [[(TERT BUTOXY)CARBONYL]AMINO] 3 [[(9H FLUOROEN 9 YLMETHOXY)CARBONYL]AMINO]PROPANOATE; METHYL 3 [[(BENZYLOXY)CARBONYL]AMINO] 2 [[(TERT BUTOXY)CARBONYL]AMINO]PROPANOATE; PROPIONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; AZA HENRY REACTION; CHEMICAL REACTION; CHIRALITY; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; PRIORITY JOURNAL; SUBSTITUTION REACTION;

EID: 80051877505     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201100013     Document Type: Article

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