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Angewandte Chemie - International Edition

Volumn 42, Issue 35, 2003, Pages 4241-4244

Highly diastereoselective oxy-Michael additions of enantiopure δ-lactol anions to nitroalkenes: Asymmetric synthesis of 1,2-amino alcohols

(4) Adderley, Nicola J a Buchanan, David J a Dixon, Darren J a Lainé, Dramane I b

a UNIVERSITY OF CAMBRIDGE (United Kingdom)

b GLAXOSMITHKLINE (United States)

Author keywords

Amino alcohols; Diastereoselectivity; Lactols; Michael addition; Nitroalkenes

Indexed keywords

ADDITION REACTIONS; ALCOHOLS; STEREOCHEMISTRY;

STEREOINDUCTION;

MOLECULAR ORIENTATION;

1,2 AMINOALCOHOL DERIVATIVE; ALKENE; AMINOALCOHOL; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

ALKENES; AMINO ALCOHOLS; ANIONS; MODELS, CHEMICAL; MOLECULAR STRUCTURE; NITRO COMPOUNDS; STEREOISOMERISM;

EID: 0141633630 PISSN: 14337851 EISSN: None Source Type: Journal
DOI: 10.1002/anie.200352007 Document Type: Article

Times cited : (51)

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