前往化源商城

The Journal of Organic Chemistry

Competing nucleophilic processes in haloalkynes. Carbanionic attacks

T Izumi, SI Miller

文献索引:Izumi,T.; Miller,S.I. Journal of Organic Chemistry, 1978 , vol. 43, # 5 p. 871 - 875

全文:HTML全文

被引用次数: 5

摘要

Carbanions (R3C-I derived from triphenylmethane and benzhydryl cyanide displace chloride ion from phenylchloroacetylene in KOH-glycol dimethyl ether (glyme) to give PhC= CCR3. Similarly, benzhydryl cyanide anion in glyme reacts with mercuric bis (ch1oroacetylide) to give the substitution product Hg (C= CCPh2CN) 2. In other cases, the" first" substitution products often react further: those of benzyl and benzhydryl cyanides are ...