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Gassman-Fentiman tool

The nature of electronic effects in cationic reactions has been probed by application of the Gassman-Fentiman tool of increasing electron demand.67 Aryl-substituted cationic centers can be made more electron demanding (i.e., electrophilic) by introduction of electron-withdrawing substituents into the aryl ring. [Pg.91]

Famum and Olah s groups have extended the so-called Gassman-Fentiman tool of increasing electron demand coupled with H and NMR spectroscopy as the structural probe under stable ion conditions to show the onset of... [Pg.236]

Gassman, P.G. Fentiman Jr., A.F. J. Am. Chem. Soc., 1969, 91, 1545 1970, 92, 2549. For a discussion of the use of the tool of increasing electron demand to probe neighboring-group activity by double bonds, sigma bonds, and aryl rings, see Lambert, J.B. Mark,... [Pg.585]

Gassman and Fentiman proposed the so-called tool of increasing electron demand of the developing cation centre For their example of the solvolysis of 7-syn-aryl-7-anti-norbomenyl-p-nitroteizoates they confirmed the -participation by three criteria ... [Pg.31]


See other pages where Gassman-Fentiman tool is mentioned: [Pg.235]    [Pg.235]    [Pg.489]   
See also in sourсe #XX -- [ Pg.91 , Pg.115 , Pg.235 , Pg.260 , Pg.266 ]

See also in sourсe #XX -- [ Pg.194 , Pg.236 ]




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