Enantioselective hydrogenation of α-aminomethylacrylates containing a free N - H group for the synthesis of β-amino acid derivatives

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 43, 2007, Pages 16787-16792

  Qiu, Liqin ^b   Prashad, Mahavir ^a   Hu, Bin ^a   Prasad, Kapa ^a   Repič, Oljan ^a   Blacklock, Thomas J ^a   Fuk, Yee Kwong ^b   Kok, Stanton H L ^b   Hang, Wai Lee ^b   Chan, Albert S C ^b  

^a NOVARTIS PHARMA AG   (Switzerland)

^b HONG KONG POLYTECHNIC UNIVERSITY   (Hong Kong)

Author keywords

Asymmetric catalysis; Baylis Hillman reaction

Indexed keywords

2 [(BENZYLAMINO)METHYL] 2 HEXENOIC ACID METHYL ESTER; 2 [(BENZYLAMINO)METHYL]HEXANOIC ACID METHYL ESTER; 2 [(BENZYLOXYAMINO)METHYL] 2 HEXENOIC ACID METHYL ESTER; 2 [(BENZYLOXYAMINO)METHYL] 3 PHENYLACRYLIC ACID METHYL ESTER; 2 [(BENZYLOXYAMINO)METHYL] 3 PHENYLPROPIONIC ACID METHYL ESTER; 2 [(BENZYLOXYAMINO)METHYL]HEXANOIC ACID METHYL ESTER; ACRYLIC ACID METHYL ESTER; ALLYL COMPOUND; BETA AMINO ACID; UNCLASSIFIED DRUG;

ACETYLATION; AMINATION; ARTICLE; BAYLIS HILLMAN REACTION; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; HYDROGENATION; PRIORITY JOURNAL; SYNTHESIS;

AMINO ACIDS; CATALYSIS; HYDROGENATION; METHACRYLATES; STEREOISOMERISM;

EID: 36749051751     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0704461104     Document Type: Article

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