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Enol triflates vinyl carbanion equivalents

X = OTf) may fail to accomplish metal exchange and consequently hinder the formation of the alke-nylchromium reagent. Few examples of the use of enol triflates as progenitors of vinyl carbanion equivalents have appeared. Consequently, the work from Takai and coworkers is particularly useful. The alkenylchromiums generated from enol triflates are functionally indistinguishable from those generated from iodoalkenes (equation 65 and table 10). This fact is disclosed by comparison of Table 9 with Table 10. [Pg.195]


See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.195 ]




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Carbanion equivalent

Carbanions enolates

Carbanions equivalents

Carbanions vinylic

Enol equivalents

Enol triflate

Enol triflates

Enol triflates vinylation

Enolate equivalents

Enolate vinylation

Enolates enolate equivalents

Enolates equivalents

Enolates triflate

Vinyl carbanions

Vinyl triflate

Vinyl triflates

Vinylic triflates

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