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Trichloroacetimidate method condensation

High a-selectivities were observed when the D-galactosyl donor 10 was used for the coupling with secondary hydroxy groups in carbohydrate acceptors including 9 (see Scheme 5). With the trichloroacetimidate method [5], the yields of disaccharides derived from 6 and 7 were 85% (10 1, a/p) and 87% (only a), respectively. The condensation of 10... [Pg.417]


See other pages where Trichloroacetimidate method condensation is mentioned: [Pg.289]    [Pg.482]    [Pg.53]    [Pg.482]    [Pg.23]    [Pg.317]    [Pg.209]    [Pg.604]    [Pg.284]    [Pg.591]    [Pg.21]    [Pg.78]   
See also in sourсe #XX -- [ Pg.4 , Pg.207 , Pg.208 ]

See also in sourсe #XX -- [ Pg.4 , Pg.207 , Pg.208 ]




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Condensation methods

Trichloroacetimidate

Trichloroacetimidate method

Trichloroacetimidates

Trichloroacetimidates method

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