One-pot conversion of 1,2-diols to epoxides: Convenient preparation of methyl 2,3-anhydro-5-O-trityl-β-D-lyxofuranoside and methyl 2,3,-anhydro-4,6-O-benzylidene-α-D-mannopyranoside

Article abstract of DOI:10.1080/00397919308009780

Tosyl chloride and sodium hydride are used to convert some 1,2-diols to epoxides in one-pot in enantiomerically/diastereomerically pure form.

Full text of DOI:10.1080/00397919308009780

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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One-Pot Conversion of 1,2-
Diols to Epoxides: Convenient
Preparation of Methyl 2,3-
Anhydro-5-O-trityl-β-D-
lyxofuranoside and Methyl 2,3-
Anhydro-4,6-O-benzylidene-α-
D-mannopyranoside
V. Srinivasa Murthy a , A. S. Gaitonde a & S. Prahlada
Rao a
a Indian Institute of Chemical Technology ,
Hyderabad, 500 007, India
Published online: 23 Sep 2006.
To cite this article: V. Srinivasa Murthy , A. S. Gaitonde & S. Prahlada Rao
(1993) One-Pot Conversion of 1,2-Diols to Epoxides: Convenient Preparation of
Methyl 2,3-Anhydro-5-O-trityl-β-D-lyxofuranoside and Methyl 2,3-Anhydro-4,6-O-
benzylidene-α-D-mannopyranoside, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 23:3, 285-289, DOI:
10.1080/00397919308009780
To link to this article: http://dx.doi.org/10.1080/00397919308009780
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