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C-Glycosides. 7. Stereospecific C-glycosylation of aromatic and heterocyclic rings

S. Czernecki, +1 more
- 01 Feb 1989 - 
- Vol. 54, Iss: 3, pp 610-612
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This article is published in Journal of Organic Chemistry.The article was published on 1989-02-01. It has received 125 citations till now. The article focuses on the topics: Glycosylation.

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Asymmetric Cu-Catalyzed Intermolecular Trifluoromethylarylation of Styrenes: Enantioselective Arylation of Benzylic Radicals

TL;DR: A novel asymmetric radical trifluoromethyl-arylation of alkenes has been developed, which provides an efficient approach to access chiral CF3-containing 1,1-diarylmethane derivatives with good to excellent enantioselectivity.
Journal ArticleDOI

Stereoselective C-Glycosylation Reactions of Ribose Derivatives: Electronic Effects of Five-Membered Ring Oxocarbenium Ions

TL;DR: The factors controlling the highly alpha-selective C-glycosylation of ribose derivatives were determined by examining the stereoselective reactions of 18 ribose analogues differing in substitution at C-2, C-3, and C-4.
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