ChemInform Abstract: Highly Functionalized Cyclopentanes by Radical Cyclization of Unsaturated Bromolactones. Part 1. Preparation of 5- Deoxycarbahexofuranoses.
β Scribed by A. M. HORNEMAN; I. LUNDT
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
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 βFull Textβ option. The original article is trackable via the βReferencesβ option.
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Highly Functionalized Cyclopentanes by Radical Cyclization of Unsaturated Bromolactones. Part 3. Preparation of Carbaaldohexofuranoses. Determination of the Relative Configuration at C-4/C-5 or 2,3-Unsaturated Heptono-1,4-lactones by Means of 1 H NMR Spectroscopy. -Key step in the synthesis of carb
5-Endo-trig Radical Cyclizations of Bromomethyldimethylsilyl Diisopropylpropargylic Ethers. A Highly Diastereoselective Access to Functionalized Cyclopentanes. -The title ethers (I), (V) and (VIII) undergo a radical-induced 5-exo-dig cyclization-diastereoselective 1,5-hydrogen transfer-5-endo-trig
## 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 βFull Textβ option. The original article is trackable v
## 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 βFull Textβ option. The original article is trackable v