Ketone Methylenation Using the Tebbe and Wittig Reagents - A Comparison
维蒂希反应
酮
试剂
外消旋化
化学
有机化学
作者
Stanley H. Pine,Gregory S. Shen,Huan Hoang
出处
期刊:Synthesis [Thieme Medical Publishers (Germany)] 日期:1991-01-01卷期号:1991 (02): 165-167被引量:79
标识
DOI:10.1055/s-1991-26406
摘要
Ketone methylenation has been accomplished using the Tebbe and the Wittig reagents. Comparison of the two reagents for a variety of ketones shows that the Tebbe reagent gives better product yields than the Wittig reagent. This is particularly important when the ketone substrate is hindered. It is also noted that the Tebbe reaction accomplishes methylenation in a non-basic medium, thus racemization does not take place on substrates with enolizable chiral centers.