4.8 Article

Stereocontrolled Photoinduced Glycosylation Using an Aryl Thiourea as an Organo photoacid

Journal

ORGANIC LETTERS
Volume 18, Issue 13, Pages 3190-3193

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01404

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) [16H01161]
  2. Strategic Research Foundation at Private Universities from Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
  3. Grants-in-Aid for Scientific Research [16J00784, 16H01161] Funding Source: KAKEN

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Photoinduced glycosylation of alcohols with alpha-glucosyl trichloroacetimidates, using aryl urea and thioureas as organo photoacids, was examined under long wavelength UV (ultraviolet) irradiation. The results show, for the first time, that such glycosylations proceed effectively to give the corresponding glycosides in high yields. In addition, high beta-stereoselectivity was obtained under high concentration conditions, whereas high alpha-stereoselectivity was realized under low concentration conditions.

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