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Organosulfur reagents

Synthetic applications of organosulfur reagents are expanding rapidly. Stable sulfuranes are included for the first time in BIS[2,-2,2-TRIPLUORO-l-PHENYL-l-(TRIFLUOROMETHYL)ETHOXY] diphenyl SULFURANE and DIETHYLAMINOSULFUR TRI-FLUORIDE. The latter is used to transform an alcohol to a fluoride in p-NITROBENZYL FLUORIDE. The direct homologation of a ketone to a nitrile by use of p-TOLYLSULFONYLMETHYL ISOCYANIDE is illustrated in 2-ADAMANTANECARBONITRILE. Reagents with... [Pg.128]

A number of synthetic applications of different classes of organosulfur compounds have already been mentioned in previous chapters. The purpose of this chapter is to highlight the major organosulfur reagents, giving their important uses in synthetic organic chemistry. [Pg.185]


See other pages where Organosulfur reagents is mentioned: [Pg.8]    [Pg.9]    [Pg.11]    [Pg.12]    [Pg.14]    [Pg.15]    [Pg.16]    [Pg.17]    [Pg.18]    [Pg.19]    [Pg.20]    [Pg.21]    [Pg.22]    [Pg.23]    [Pg.24]    [Pg.25]    [Pg.26]    [Pg.27]    [Pg.28]    [Pg.29]    [Pg.30]    [Pg.31]    [Pg.32]    [Pg.110]    [Pg.115]    [Pg.516]    [Pg.157]    [Pg.124]    [Pg.516]    [Pg.3]    [Pg.4]    [Pg.6]    [Pg.8]    [Pg.10]    [Pg.12]    [Pg.14]    [Pg.16]    [Pg.18]    [Pg.20]    [Pg.22]    [Pg.24]    [Pg.26]   


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Organosulfur

Organosulfurs

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