Stereospecific C-β-glycosidation and synthesis of 4,7-anhydro-5,6-isopropylidene-4 (S), 5(S), 6(R), 7(R)-tetrahydroxyoxocan-2-one

Article abstract of DOI:10.1080/00397919308011209

Wittig reaction of 2,3-0-isopropylidene-5-0-P-anisyldiphenylmethyl-β-D-ribofuranose (2) with methoxycarbonyl-methylene triphenylphosphorane was accompanied by spontaneous cyclization to generate 3 stereospecifically. Deprotection of 5-OH followed by mild

Full text of DOI:10.1080/00397919308011209

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Synthetic Communications: An
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Organic Chemistry
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Stereospecific C=β-
Glycosidation and Synthesis
of 4,7-Anhydro-5,6-
isopropylidene-4
(S), 5(S), 6(R), 7(R)-
Tetrahydroxyoxocan-2-one
Sukhendu B. Mandal a & Basudeb Achari a
a Indian Institute of Chemical Biology, Calcutta,
700032, India
Published online: 24 Sep 2006.
To cite this article: Sukhendu B. Mandal & Basudeb Achari (1993) Stereospecific
C=β-Glycosidation and Synthesis of 4,7-Anhydro-5,6-isopropylidene-4 (S), 5(S), 6(R),
7(R)-Tetrahydroxyoxocan-2-one, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 23:9, 1239-1244, DOI:
10.1080/00397919308011209
To link to this article: http://dx.doi.org/10.1080/00397919308011209
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