A stereocontrolled synthetic route to anti-beta-amino alcohols
A physiologically indispensable beta -amino hydroxy functionality has been constructed with complete anti-stereoselectivity by intramolecular iodoamidation of (Z)-olefinic homoallylic trichloroacetimidates 4-6, 18, 20, 30 and 32, which comprise bulky substituents at the vinylic positions. (C) 2001 Elsevier Science Ltd. All rights reserved.
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Issue Date
- 2001-10
- Language
- English
- Article Type
- Article
- Keywords
ASYMMETRIC-SYNTHESIS; ENANTIOCONTROLLED SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; ACIDS; COMPLEXES; CATALYST; ESTERS
- Citation
TETRAHEDRON LETTERS, v.42, no.43, pp.7599 - 7603
- ISSN
- 0040-4039
- Appears in Collection
- CH-Journal Papers(저널논문)
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