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Highly Stereoselective 1,4-Conjugate Addition of Organocopper Reagents to Methyl α- d -Glucopyranoside Derivatives Tethering an Unsaturated Ester Moiety at C-4 or C-6 1

✍ Scribed by Totani, Kiichiro; Nagatsuka, Takayuki; Takao, Ken-ichi; Ohba, Shigeru; Tadano, Kin-ichi

Book ID: 127355617
Publisher: American Chemical Society
Year: 1999
Tongue: English
Weight: 149 KB
Volume: 1
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol9909942

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ChemInform Abstract: Highly Stereoselect

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective Lewis Acid Mediated Conjugate Radical Additions to Methyl α-D-Glucopyranoside Derivatives Tethering an Unsaturated Ester Moiety at C-4.

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