Bulletin of the Chemical Society of Japan p. 3440 - 3443 (1993)
Update date:2022-08-02
Topics:
Yoshifuji, Masaaki
Kamijo, Kazunori
Toyota, Kozo
A sterically hindered bromobenzene, 2-bromo-1,5-di-t-butyl-3-(methoxymethyl)benzene, was prepared and converted to the corresponding phosphonous dichloride.The dichloride was then utilized to stabilize a low-coordinate phosphorus compound such as 1-<2,4-di-t-butyl-6-(methoxymethyl)phenyl-2-(2,4,6-tri-t-butylphenyl)diphosphene.Furthermore, the dichloride gave a cyclization product 1-chloro-2,1-oxophosphaindan with elimination of chloromethane on standing at room temperature.
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Doi:10.3762/bjoc.10.114
(2014)Doi:10.1016/j.ejmech.2016.05.041
(2016)Doi:10.1002/recl.19931121002
(1993)Doi:10.1016/S0040-4039(00)73940-2
(1993)Doi:10.1016/S0008-6215(01)00323-8
(2002)Doi:10.1039/c39940000365
(1994)