Diastereoconvergent synthesis of anti-1,2-amino alcohols with N-containing quaternary stereocenters via selenium-catalyzed intermolecular C–H amination
Author:
Affiliation:
1. Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700, USA
Abstract
Funder
National Science Foundation
University of Washington
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/SC/D2SC02648A
Reference54 articles.
1. Synthesis of Physiologically Potent β-Amino Alcohols
2. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds
3. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis
4. Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion
5. C–H functionalization logic in total synthesis
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