Chemistry Letters p. 867 - 870 (1990)
Update date:2022-07-29
Topics:
Wada, Masanori
Kanzaki, Mituyuki
Fujiwara, Masanobu
Kajihara, Kazuhisa
Erabi, Tatsuo
Tris(2,6-dimethoxyphenyl)phosphine sulfide reacted with alkyl iodides or bromides under mild conditions to give stable alkylthiophosphonium salts, which reacted with thiols at room temperature in the presence of a catalytic amount of tris(2,6-dimethoxyphenyl)phosphine to give the tertiary phosphonium salt and unsymmetrical disulfides.
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