z-logo
Premium
Use of β,γ‐Unsaturated α‐Ketocarbonyls for a Totally Regioselective Oxidative Multicomponent Synthesis of Polyfunctionalized Pyridines
Author(s) -
Allais Christophe,
Constantieux Thierry,
Rodriguez Jean
Publication year - 2009
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200902491
Subject(s) - regioselectivity , oxidative phosphorylation , chemistry , combinatorial chemistry , organic chemistry , biochemistry , catalysis
Versatile partners : α‐Ketocarbonyls have been shown for the first time to be versatile partners in a Michael addition promoted oxidative domino three‐component reaction under heterogeneous conditions. This multicomponent reaction sequence led to the development of a general synthesis of highly functionalized pyridines (see scheme), allowing selective and simultaneous incorporation of a substituent at the 4‐position and a synthetically useful functionality at the strategic 2‐position.

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