Journal of the Chemical Society. Perkin transactions I p. 2239 - 2244 (1981)
Update date:2022-09-26
Topics:
Dahl, Britta M.
Dahl, Otto
Trippett, Stuart
Starting from lithium o-lithiobenzyl alkoxides and dichlorophosphines, a series of P-substituted 3H-2,1-benzoxaphospholes has been prepared and converted into five-co-ordinate phosphoranes by addition of 4,5-dimethyl-o-benzoquinone or 4,4'-dimethylbenzil, or condensation with 4,5-dimethylpyrocatechol or pinacol.The varieble-temperature n.m.r. spectra of these phosphoranes are discussed.In these systems phenylamino- and dimethylamino-groups have similar apicophilicities and are less apicophilic than hydrogen by some 4-5 kcal mol-1.
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Doi:10.1021/ja00410a041
(1981)Doi:10.1055/s-0034-1378739
(2015)Doi:10.1016/S0040-4020(01)92090-3
(1981)Doi:10.1016/S0008-6215(00)80765-X
(1981)Doi:10.1016/S0022-328X(00)00635-5
(2001)Doi:10.1021/jm00144a004
(1981)
