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Tributylstannyllithium reactions

Aldehydes and a-bromo ketones or esters are efficiently coupled in an aldol reaction in the presence of Diethylalu-minum Chloride-Tributylstannyllithium (or Tin(II) Chloride)... [Pg.469]

Preparative Methods most conveniently prepared by reacting tributylstannyllithium with commercially available 2-chloromethyl-3-trimethylsilyl-l-propene, although methods involving reaction of the dithiocarbamate or allylic sulfide derived from 2-trimethylsilylmethylprop-2-en-ol with BusSnH and AIBN have been reported. ... [Pg.731]

Scheme 2.87. The Peterson reaction of a-silyl carbanions generated by reduction of a sulfanyl group with tributylstannyllithium. Scheme 2.87. The Peterson reaction of a-silyl carbanions generated by reduction of a sulfanyl group with tributylstannyllithium.
See other pages where Tributylstannyllithium reactions is mentioned: [Pg.566]    [Pg.195]    [Pg.552]   
See also in sourсe #XX -- [ Pg.314 ]



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Tributylstannyllithium

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