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Glycoside synthesis unprotected donors

The notion of glycoside synthesis with unprotected glycosyl donors [10] has instigated the exploration of some new approaches using the trichloroacetimidate group [15], electrochemistry [16], electron transfer [17], and Lewis acid catalysis [18], The scope of applicability of these newer methods remains to be tested. [Pg.385]

B. General procedures for the synthesis of 1,2-cis-glycosides from unprotected MOP donors 401... [Pg.389]

Scheme 2 Synthesis of 1,2-cir glycosides with unprotected MOP-glycosyl donors. Scheme 2 Synthesis of 1,2-cir glycosides with unprotected MOP-glycosyl donors.
Scheme 3 l,2-/rcwj-Glycoside synthesis using an unprotected MOP glycosyl donor containing a 2-acetamido group. [Pg.393]

B. General Procedures for the Synthesis of 1,2-c/s-Glycosides from Unprotected MOP Donors... [Pg.538]

V. Ferrieres, J.-N. Bertho, and D. Plusquellec, A new synthesis of 0-glycosides from totally O-unprotected glycosyl donors, Tetrahedron Lett. 36 2749 (1995). [Pg.388]

Glycoside and Oligosaccharide Synthesis with Unprotected Glycosyl Donors Based on the Remote Activation Concept... [Pg.389]

II. Glycoside and Oligosaccharide Synthesis Using 3-Methoxy-2-pyridyloxy (MOP) O-Unprotected Glycosyl Donors 391... [Pg.389]

See other pages where Glycoside synthesis unprotected donors is mentioned: [Pg.34]    [Pg.292]    [Pg.386]    [Pg.390]    [Pg.415]    [Pg.432]    [Pg.488]    [Pg.200]    [Pg.202]    [Pg.223]    [Pg.545]    [Pg.46]    [Pg.46]    [Pg.200]    [Pg.202]    [Pg.223]    [Pg.545]    [Pg.224]    [Pg.199]    [Pg.46]    [Pg.46]    [Pg.214]    [Pg.87]    [Pg.295]    [Pg.119]    [Pg.138]    [Pg.896]    [Pg.263]    [Pg.285]    [Pg.452]    [Pg.452]    [Pg.63]    [Pg.760]    [Pg.783]   
See also in sourсe #XX -- [ Pg.389 ]



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