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Disilyl dithiophosphonates in the synthesis of open chain and cyclic organothiophosphorus compounds

✍ Scribed by Il'yas S. Nizamov; Gul'nur G. Sergeenko; Il'nar D. Nizamov; Yan E. Popovich; Ravil N. Khaibullin; Lyubov A. Al'metkina; Boris E. Abalonin; Elvira S. Batyeva; Dmitry B. Krivolapov; Igor A. Litvinov


Book ID
102228021
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
134 KB
Volume
15
Category
Article
ISSN
1042-7163

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✦ Synopsis


Abstract

O‐(Trimethylsiloxy)alkyl S‐trimethylsilyl aryldithiophosphonates 7a–d were obtained by the reaction of 2,4‐diaryl‐1,3,2,4‐dithiadiphosphetane‐2,4‐disulfides 5a,b with disilyl derivatives of glycols 6a,c and salicyl alcohol 6b. The reactions of mixed O,S‐bis(trimethylsilyl) 2,4‐di(3,5‐di‐tert‐butyl‐4‐hydroxyphenyl)dithiophosphonate 1 and S‐silyl aryldithiophosphonates 7a,b with S,S‐diethyldithiodiphenylgermane 2, dichlorodiphenylgermane 8a, and dichlorodiphenylstannane 8b were studied. The structure of hexaphenyl‐2,4,6,1,3,5‐trithiatrigerminane 11 was established by X‐ray single crystal diffraction. © 2004 Wiley Periodicals, Inc. Heteroatom Chem 15:225–232, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20009


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