Hydrogenolysis of dioxolane-type benzylidene derivatives: a convenient preparation of methyl 2-O-benzyl- and 3-O-benzyl-4,6-O-benzylidene-α-d-mannopyranoside-Reference-Cited by-同舟云学术

Hydrogenolysis of dioxolane-type benzylidene derivatives: a convenient preparation of methyl 2-O-benzyl- and 3-O-benzyl-4,6-O-benzylidene-α-d-mannopyranoside

Published:1979-08 Issue:1 Volume:73 Page:327-331
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Lipták András,Czégény Ildikó,Harangi János,Nánási Pál

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference18 articles.

1. Use of the benzyl group during purdie methylation: a synthesis of 2-O-methyl-D-mannose

2. Synthesis of 6-deoxy-1,2:3,5-di-O-methylidene-α-D-xylo-hex-5-enofuranose

3. Hydrogenolysis of carbohydrate acetals, ketals, and cyclic orthoesters with lithium aluminium hydride – aluminium trichloride

4. Organotin derivatives and the selective acylation and alkylation of the equatorial hydroxy group in a vicinal, equatorial-axial pair

5. An improved method for selective substitution on O-3 of D-mannose. Application to the synthesis of methyl 3-O-methyl-and 2-O-α-Dmannopyranosides

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