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Stannanes reactions with thioacetals

Williams and coworkers have expanded the utility of this methodology via the application to highly functionalized substrates. transmetalation with R.R)-ot (S,S)-228 is quantitative and dependable, with a variety of allylic stannanes with C-2 substitution. Carbon chains at C-2 of the allyl component may contain additional functionality, including benzyl and allyl ethers, silyl ethers, esters, alkenes, halogens, or thioacetals, as well as stereogeificity. Asymmetric induction in the condensation with aldehydes is dominated by the chiral auxiliary. In this fashion, the allylation reaction may be designed as a convergent... [Pg.538]


See also in sourсe #XX -- [ Pg.58 , Pg.963 ]

See also in sourсe #XX -- [ Pg.58 , Pg.963 ]

See also in sourсe #XX -- [ Pg.478 ]




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Reactions thioacetalization

Stannane reactions

Stannanes reactions

Stannanes reactions with

Thioacetal

Thioacetalization

Thioacetate

Thioacetates

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