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Synlett 1993; 1993(8): 561-563
DOI: 10.1055/s-1993-22528
DOI: 10.1055/s-1993-22528
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Enhancing Stereoselectivity from Reactions with Modest Group Selectivity
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Publikationsverlauf
Publikationsdatum:
19. März 2002 (online)
Analysis of the kinetics of certain group selective processes reveals that reactions with only modest group selectivity (3-4:1) can lead to modest yields (50%) of products with high stereoisomeric purity (10-20:1). The analysis is verified by the selective reduction of galacto- and D-gluco-hexanedials with B-isopinocampheyl-9-borabicyclo-[3.3.1]nonane (Alpine-Borane®) to give the D-galacto-, L-galacto-, D-gluco-, and L-gulo-hydroxyaldehydes.