(PDF) Phenyl 4,6-Di-O-Acetyl-2,3-Dideoxy

Phenyl 4,6-Di-O-Acetyl-2,3-Dideoxy-1-Thio-Α-D-Erythro-Hex-2-Enopyranoside

Acta Crystallographica Section E Structure Reports Online

doi 10.1107/s1600536811040165

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Abstract

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Date

October 5, 2011

Authors

Henok H. Kinfe

Fanuel M. Mebrahtu

Alfred Muller

Publisher

International Union of Crystallography (IUCr)

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Concerning the Mechanism of the Reaction of Methyllithium With Methyl 2,3-Anhydro-4,6-O-Benzylidene-Α-D-Allopyranoside to Form 4,6-O-Benzylidene- 1,2-Didehydro-1,2-Dideoxy-2-Methyl-D-Ribo-Hexopyranose

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(E)-1-(4-Chlorophenyl)-3-[4-(2,3,4,6-Tetra-O-Acetyl-Β-D-Allopyranosyloxy)phenyl]prop-2-En-1-One

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Phenyl 4,6-Di-O-Acetyl-2,3-Dideoxy-1-Thio-Α-D-Erythro-Hex-2-Enopyranoside

Acta Crystallographica Section E Structure Reports Online

doi 10.1107/s1600536811040165

Full Text

Abstract

Date

Authors

Publisher

Related search

Base-Catalyzed Degradations of Carbohydrates. IV. Formation of 2,3-Anhydro-2-Methoxy-Α-D-Allopyranose Derivatives From 3-Deoxy-D-Erythro-Hex-2-Enopyranoses

Concerning the Mechanism of the Reaction of Methyllithium With Methyl 2,3-Anhydro-4,6-O-Benzylidene-Α-D-Allopyranoside to Form 4,6-O-Benzylidene- 1,2-Didehydro-1,2-Dideoxy-2-Methyl-D-Ribo-Hexopyranose

1-O-Acetyl-3,4,6-Tri-O-Benzyl-2-C-Bromomethyl-2-Deoxy-Α-D-Glucopyranose

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