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STUDIES ON GLYCOSIDES XⅢ.──HIGHLY STEREOSELECTIVE SYNTHESIS OF PER-O-BENZYLATED O-,S-α-D-GALACTOPYRANOSIDES AND GALACTOSYL CARBOXYUTES FROM PER-O-BENZYIATED GALACTOSYL TRIFLUOROACETATE

STUDIES ON GLYCOSIDES XⅢ.──HIGHLY STEREOSELECTIVE SYNTHESIS OF PER-O-BENZYLATED O-,S-α-D-GALACTOPYRANOSIDES AND GALACTOSYL CARBOXYUTES FROM PER-O-BENZYIATED GALACTOSYL TRIFLUOROACETATE
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摘要 s: a Linked O- and S-galactopyranosides, and galactopyranosyl carbexylates were synthesized as the sole products from 2.3,4,6-tetra-O-benzyl-1-trifluoroacetyl-a-D-galacto-pyranose (2). The behavior of the nucleophiles and the two kinds of catalysts (BF3.OEt2 and TMSOTf) were discussed. s: a Linked O- and S-galactopyranosides, and galactopyranosyl carbexylates were synthesized as the sole products from 2.3,4,6-tetra-O-benzyl-1-trifluoroacetyl-a-D-galacto-pyranose (2). The behavior of the nucleophiles and the two kinds of catalysts (BF3.OEt2 and TMSOTf) were discussed.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 1994年第6期465-466,共2页 中国化学快报(英文版)
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