The Oxidation of Organocuprates — An Offbeat Strategy for Synthesis
✍ Scribed by David S. Surry; David R. Spring
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 8 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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## Abstract A practical and highly regio‐ and stereoselective synthesis of oligoprenols starting from commercially available geraniol is described. The convergent synthetic strategy features the iterative allyl‐allyl coupling of monomers easily derived from geraniol that contain one reacting termin
We thank Dr. Paul A. Lartey (Abbott Laboratories) for a generous gift of erythromycin A for use as a source of d-desosamine and l-cladinose, and we are grateful to Dr. Erica Kraynack and Dr. Philippe Breton for conducting exploratory glycosylation studies.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.