A regio- and stereodivergent synthesis of vic-amino alcohols
2000 (English)In: Organic Letters, ISSN 1523-7060, E-ISSN 1523-7052, Vol. 2, no 25, 4087-4089 p.Article in journal (Refereed) Published
[GRAPHICS] A regio- and stereodivergent synthesis of vic-amino alcohols starting from vinylepoxides is described. The developed strategy focuses on the propensity of vinylepoxides and vinylaziridines to be ring-opened at the allylic position by suitable nucleophiles and makes use of reactions that perform such tasks selectively with either retention or inversion of configuration.
Place, publisher, year, edition, pages
2000. Vol. 2, no 25, 4087-4089 p.
asymmetric-synthesis, 1,2-amino alcohols, beta-amino, enantioselective synthesis, opening reaction, building-blocks, aziridines, efficient, rearrangement, epoxides
IdentifiersURN: urn:nbn:se:kth:diva-20215DOI: 10.1021/ol006736iISI: 000165829200035OAI: oai:DiVA.org:kth-20215DiVA: diva2:338908
QC 201005252010-08-102010-08-10Bibliographically approved