
Bulletin of the Chemical Society of Japan p. 361 - 362 (1983)
Update date:2022-09-26
Topics:
Akiyama, Shuzo
Nakatsuji, Shin'ichi
Yoshida, Keiko
Nakashima, Kenichiro
Hagiwara, Toshimitsu
et al.
Two convenient methods for the preparation of p-dialkylaminophenylacetylenes are reported: a) Dehydrobromination of the brominated compounds obtained easily from the dialkylamino substituted cinnamic acids in acetic acid instead of chloroform; b) dehydrochlorination of the 2-chlorostyrene derivative obtained from the reaction of p-dimethylaminobenzaldehyde with chloromethylenetriphenylphosphorane.
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Doi:10.1021/ja01106a015
(1953)Doi:10.1002/ejoc.200400891
(2005)Doi:10.1246/bcsj.56.792
(1983)Doi:10.1021/jo0502091
(2005)Doi:10.1139/v73-225
(1973)Doi:10.1021/jo00161a011
(1983)