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Michael addition carbon-sulfur bond formation

Chen C, Lin Y, Liu C. Catal3dic carbon-sulfur bond formation by amphoteric vanadyl trifiate exploring with thia-Michael addition, thioacetalization, and transacetalization reactions. Tetrahedron 2009 65 10470-10476. [Pg.1439]

The asymmetric Michael addition represents one of the most powerful methods for the formation of C-X (X = C, N, O, S) bonds in organic synthesis. Chiral aluminium complex-catalysed asymmetric Michael additions will be introduced on the basis of different nucleophiles, including carbon-, nitrogen-, ojygen-, sulfur-, and phospha-based nucleophiles. [Pg.176]

See other pages where Michael addition carbon-sulfur bond formation is mentioned: [Pg.59]    [Pg.69]    [Pg.234]    [Pg.704]    [Pg.207]    [Pg.704]    [Pg.493]    [Pg.243]   
See also in sourсe #XX -- [ Pg.1415 , Pg.1417 , Pg.1418 , Pg.1419 ]



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Additives carbon

Carbon addition

Carbon sulfur

Carbon-sulfur bond

Michael addition formation

Sulfur bonding

Sulfur bonds

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