A short, convenient synthesis of enantiomerically pure N-protected 2-azanorbornane-3-carboxaldehydes and related amino alcohols

Synthesis

Volumn , Issue 14, 2002, Pages 2037-2042

  Genov, Miroslav ^a   Scherer, Gerd ^a   Studer, Martin ^b   Pfaltz, Andreas ^a  

^a UNIVERSITY OF BASEL   (Switzerland)

^b SOLVIAS AG   (Switzerland)

Author keywords

Amino alcohols; Amino aldehydes; Asymmetric Pt catalyzed hydrogenation; Asymmetric synthesis; Aza Diels Alder reaction

Indexed keywords

ALCOHOLS; ALDEHYDES; CATALYSIS; HYDROGENATION; PLATINUM;

DIASTEREOSELECTIVITY;

SYNTHESIS (CHEMICAL);

2 AZANORBORNANE 3 CARBOXALDEHYDE DERIVATIVE; AMINO ACID DERIVATIVE; AMINOALCOHOL; BIS(1 PHENYLETHYL)IMINE; BORNANE DERIVATIVE; BROMINE DERIVATIVE; CYCLOPENTADIENE DERIVATIVE; IMINE; PLATINUM; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIASTEREOISOMER; ENANTIOMER; HYDROGENATION; REACTION ANALYSIS; SYNTHESIS;

EID: 0036401976     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-34365     Document Type: Article

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