Work

Highly diastereoselective synthesis of β-amino alcohols

Year: 2001

Type: article

Abstract: Several substituted β-amino alcohols 1 were synthesised in a diastereoselective manner via the novel highly versatile intermediate 8b, involving a combination of N-acyliminium ion and Weinreb amide chemistry.

Source: Journal of the Chemical Society Perkin Transactions 1

DOI: 10.1039/b108254j

Authors: Wim J. N. Meester, Rudmer van Dijk, Jan H. van Maarseveen, Floris P. J. T. Rutjes, Pedro H. H. Hermkens, Henk Hiemstra

Institutions: University of Amsterdam, Radboud University Nijmegen, Organon (Netherlands)

Language: English

Topic: Asymmetric Synthesis and Catalysis

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: green

Funder: Nederlandse Organisatie voor Wetenschappelijk Onderzoek

OpenAlex ID: W2043777222

FWCI: 0.515

Cites: 11

Cited by: 10

Related to: 10