Stereochemical control in radical cyclization routes to N-glycosides: role of protecting groups and of the configuration (E versus Z) of the acceptors-Reference-Cited by-同舟云学术

Stereochemical control in radical cyclization routes to N-glycosides: role of protecting groups and of the configuration (E versus Z) of the acceptors

Published:2003-10 Issue:19 Volume:14 Page:2939-2959
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Rhee Jong Uk,Bliss Brian I.,RajanBabu T.V.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference29 articles.

1. A New Reaction Manifold for the Barton Radical Intermediates: Synthesis of N-Heterocyclic Furanosides and Pyranosides via the Formation of the C1−C2 Bond

2. Radical cyclizations of xanthates without deoxygenation have been reported. See: (a) Bachi, M. D.; Bosch, E. J. Chem. Soc., Perkin Trans. 1 1988, 1517;

3. (b) Nozaki, K.; Oshima, K.; Utimoto, K. Tetrahedron Lett. 1988, 29, 6127;

4. (c) Yamamoto, M.; Uruma, T.; Iwasa, S.; Kohmoto, S.; Yamada, K. J. Chem. Soc., Chem. Commun. 1989, 1265;

5. (d) Use of thioimidazolide: Angoh, A. G.; Clive, D. L. J. J. Chem. Soc., Chem. Commun. 1985, 980.

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