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Sulfonamides trapping reagents

C.viii. Amines, Amides, Imides, and Sulfonamides as the H—Y Trapping Reagents Intermolecular Diene Dimerization... [Pg.1602]

Scheme 3.48. Sulfonamide/CuX-catalyzed addition of dialkylzinc reagents to 2-enones and subsequent trapping of the zinc enolates [199a-bj. Scheme 3.48. Sulfonamide/CuX-catalyzed addition of dialkylzinc reagents to 2-enones and subsequent trapping of the zinc enolates [199a-bj.
Sulfonyl azides participate in unique CuAAC reactions with terminal alkynes. Depending on the conditions and reagents, products other than the expected triazole 20 [118] can be obtained, as shown in Scheme 7.9. For example, N-sulfonyl azides are converted to N-sulfonyl amidines 21 when the reaction is conducted in the presence of amines [119]. In the aqueous conditions, N-acyl sulfonamides 22 are the major products [120,121]. In addition to amines and water, the latter can be trapped with imines, furnishing N-sulfonyl azetidinimines 23 [122]. [Pg.215]


See other pages where Sulfonamides trapping reagents is mentioned: [Pg.1588]    [Pg.126]    [Pg.126]    [Pg.126]    [Pg.266]    [Pg.72]    [Pg.126]    [Pg.401]    [Pg.28]   
See also in sourсe #XX -- [ Pg.1602 , Pg.1603 , Pg.1604 ]




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Trapping reagent

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