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Synthesis and reactions of diphosphenes carrying bulky aryl and phenoxy groups

โœ Scribed by De-Lie An; Kozo Toyota; Masafumi Yasunami; Masaaki Yoshifuji


Book ID
102847418
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
766 KB
Volume
6
Category
Article
ISSN
1042-7163

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โœฆ Synopsis


Unsymmetrical diphosphenes carrying bulky alyl and phenoxy groups were prepared by the reaction of lithium 2,4,6-tri-t-butylphenylphosphide with the corresponding phenyl phosphorodichbridites, followed by the dehydrochlorination reaction with 1,g-diazabicyclo[5.4.0]undec-7-ene. The diphosphenes were isolated as stable compounds. The reactions of these diphosphenes with elemental sulfur or selenium afforded the corresponding thiadiphosphiranes or seknadiphosphiranes, respectively. The diphosphenes also reacted with dichlorocarbene to give dichlorodiphosph iranes .


๐Ÿ“œ SIMILAR VOLUMES


Synthesis and redox properties of a diph
โœ Kyoko Tsuji; Shigeru Sasaki; Masaaki Yoshifuji ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 274 KB

The 2,6-dimesityl-4-[bis(4-methoxyphenyl)amino]phenyl group was developed as a sterically protecting group carrying a reversible redox site at the 4-position and was applied to the construction of a novel redox system composed of the diphosphene and triarylamine units.