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VAN LEUSEN Reagent

VAN LEUSEN Reagent 397 VEDEJS Hydroxylation 398 Venketaraman 14 Verisy 251 VHIiger 13 Vnhe 399... [Pg.227]

Substituted oxazoles through the reaction of -toIyIsulfonylmethyl isocyanide (TosMIC, also known as the van Leusen reagent) with aldehydes in protic solvents at refluxing temperatures. [Pg.556]

Van Leusen and Wildeman101 have realized a 1,3-thiazole synthesis, using the reagent TosMIC (tosylmethyl isocyanate) (56)102 and CS2. [Pg.193]

An interesting approach to incorporate acrylonitrile substructures into morphinans is the van Leusen homologation reaction in which the standard reagent... [Pg.71]

In 1972 van Leusen described a simple synthesis of 4-phenylpyrroles bearing a cyano-, a keto- or an ester-group in the 3-position of the pyrrole ring, using TosMIC (5) as a key reagent (Scheme 15.2.1) [12]. [Pg.569]

See other pages where VAN LEUSEN Reagent is mentioned: [Pg.397]    [Pg.432]    [Pg.388]    [Pg.432]    [Pg.433]    [Pg.388]    [Pg.397]    [Pg.432]    [Pg.388]    [Pg.432]    [Pg.433]    [Pg.388]    [Pg.259]    [Pg.602]    [Pg.119]    [Pg.74]    [Pg.239]    [Pg.344]    [Pg.390]    [Pg.390]    [Pg.557]    [Pg.614]    [Pg.557]   
See also in sourсe #XX -- [ Pg.397 ]

See also in sourсe #XX -- [ Pg.388 ]

See also in sourсe #XX -- [ Pg.556 ]

See also in sourсe #XX -- [ Pg.613 ]

See also in sourсe #XX -- [ Pg.388 ]

See also in sourсe #XX -- [ Pg.556 ]



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