z-logo
Premium
Catalytic Enantioselective Alkylation of Substituted Dioxanone Enol Ethers: Ready Access to C(α)‐Tetrasubstituted Hydroxyketones, Acids, and Esters
Author(s) -
Seto Masaki,
Roizen Jennifer L.,
Stoltz Brian M.
Publication year - 2008
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200801424
Subject(s) - enantioselective synthesis , alkylation , enol , stereocenter , catalysis , chemistry , organic chemistry , combinatorial chemistry
Adaptive Alkylation : Palladium‐catalyzed asymmetric alkylation enables access to fully substituted enantioenriched oxygenated stereocenters, which can be transformed easily to α‐hydroxyketones, esters, and acids, providing a catalytic, enantioselective synthesis for natural products.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom