Photochemical reactions of imidazole-1-sulfonates (imidazylates)

Article abstract of DOI:10.1080/07328309808002900

Imidazylates 1-3 were irradiated in methanol in the presence and in the absence of the electron donor triethylamine. In each case photochemical deprotection occurred in excellent yield to form the partially protected sugar from which the imidazylate was synthesized. Reactions in the presence of triethylamine required much shorter irradiation times.

Full text of DOI:10.1080/07328309808002900

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Journal of Carbohydrate Chemistry
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Photochemical Reactions of Imidazole-1-
Sulfonates (Imidazylates)
Shaoming Duan a , Roger W. Binkley a & Edith R. Binkley b
a Department of Chemistry, Cleveland State University, Cleveland,
Ohio, 44115
b Center for Carbohydrate Study, Oberlin, Ohio, 44074
Published online: 15 Aug 2006.
To cite this article: Shaoming Duan , Roger W. Binkley & Edith R. Binkley (1998) Photochemical
Reactions of Imidazole-1-Sulfonates (Imidazylates), Journal of Carbohydrate Chemistry, 17:3, 391-396,
DOI: 10.1080/07328309808002900
To link to this article: http://dx.doi.org/10.1080/07328309808002900
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