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Related reagents anion trap

The use of carbon nucleophiles stabilized by SR groups has been a feature of sulphur chemistry for many years now, and this year has seen additional uses for these versatile reagents. Thus the carbanion CH(SPh)2 adds in a 1,2-manner to 2-methylacrolein giving the allyl alcohol (175), which is then converted to the activated diene (176) by standard methodology. The latter has been used in studies towards the total synthesis of the Rubradirin antibiotics. The related anion ArC(SPh)2 also adds to a,/3-unsaturated systems however, in the case of lactone (177) conjugate addition is observed. If the initial ion from (177) is trapped with benzylic bromides then frans-butyrolactones (178) are obtained in good yield. ... [Pg.271]


See other pages where Related reagents anion trap is mentioned: [Pg.251]    [Pg.783]    [Pg.323]    [Pg.403]    [Pg.333]    [Pg.333]    [Pg.390]    [Pg.83]    [Pg.23]    [Pg.67]    [Pg.54]    [Pg.74]    [Pg.149]    [Pg.61]    [Pg.54]    [Pg.27]   
See also in sourсe #XX -- [ Pg.85 ]




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Anionic reagents

Related reagents

Trap anion

Trapping reagent

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