An improved bidentate complex of iridium as a catalyst for hydrogen isotope exchange

被引:17
|
作者
Herbert, JM [1 ]
Kohler, AD [1 ]
McNeill, AH [1 ]
机构
[1] Sanofi Aventis, Isotope Chem & Metabolite Synth Dept, Alnwick NE66 2JH, Northd, England
来源
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS | 2005年 / 48卷 / 04期
关键词
iridium complexes; deuterium exchange; isotope exchange;
D O I
10.1002/jlcr.921
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Iridium(l) complexes 1, containing bidentate phosphines, and 3, with arsine ligands, are generated in situ. These species mediate hydrogen isotope exchange in a variety of aromatic substrates including benzyl ketones. Although the catalytic activities of complexes 1 and 3 are generally unexceptional, a logical step leads to the use of [ethylene-1,2-bis(diphenylarsine)](cyclooctadiene)iridium(I) tetrafluoroborate (5), which is an efficient catalyst for both aryl and benzyl ketones, and mediates exchange to a. substantial extent in other substrates also. Copyright (c) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:285 / 294
页数:10
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