Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
about
C-H bond halogenation catalyzed or mediated by copper: an overviewThe [F]2-Fluoro-1,3-thiazolyl Moiety - an Easily-Accessible Structural Motif for Prospective Molecular Imaging Radiotracers.Syntheses of 2-amino and 2-halothiazole derivatives as high-affinity metabotropic glutamate receptor subtype 5 ligands and potential radioligands for in vivo imaging.Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers.
P2860
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@en
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@nl
type
label
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@en
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@nl
prefLabel
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@en
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@nl
P2093
P2860
P356
P1476
Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts.
@en
P2093
Fabrice G Siméon
Matthew T Wendahl
Victor W Pike
P2860
P304
P356
10.1021/JO802799C
P407
P577
2009-03-01T00:00:00Z