The Action of Grignard Reagents on Diaryl Phosphinyl Chlorides1
DC Morrison
Index: Morrison Journal of the American Chemical Society, 1950 , vol. 72, p. 4820
Full Text: HTML
Citation Number: 13
Abstract
This reaction of the diary1 phosphinyl chlo-rides can be compared to the reaction of Grignard reagents with sulfonyl chlorides which produces sulfones. 2 Unlike the lattex, however, no hdo-genation was observed in the reaction with phosphinyl chlorides. This may be due to the fact that both the phosphine oxides and phosphinic acids are very stable compounds and difficult to reduce.
Related Articles:
[Yuanyao Xu; Zhong Li; Jiazhi Xia; Huiju Guo; Yaozeng Huang Synthesis, 1984 , # 9 p. 781 - 782]
[Ngwendson, Julius N.; Schultze, Cassandra M.; Bollinger, Jordan W.; Banerjee, Anamitro Canadian Journal of Chemistry, 2008 , vol. 86, # 7 p. 668 - 675]
[Dalpozzo, Renato; De Nino, Antonio; Miele, Daniela; Tagarelli, Antonio; Bartoli, Giuseppe European Journal of Organic Chemistry, 1999 , # 9 p. 2299 - 2301]
[Cardellicchio, Cosimo; Fiandanese, Vito; Naso, Francesco; Pietrusiewicz, K. Michal; Wisniewski, Witold Tetrahedron Letters, 1993 , vol. 34, # 19 p. 3135 - 3138]
[Beznosko, B. K.; Usanova, V. M.; Zhuravleva, L. V.; Kharitonov, A. V.; Bondarenko, N. A.; et al. Pharmaceutical Chemistry Journal, 1990 , vol. 24, # 4 p. 244 - 247 Khimiko-Farmatsevticheskii Zhurnal, 1990 , vol. 24, # 4 p. 22 - 23]