## 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.
Stereoselective total synthesis of cytotoxic sporiolide A
β Scribed by D. Kumar Reddy; K. Rajesh; V. Shekhar; D. Chanti Babu; Y. Venkateswarlu
- Book ID
- 104098198
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 241 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A simple and highly efficient stereoselective total synthesis of cytotoxic agent sporiolide A has been achieved starting from D-mannitol; the strategy of synthesis utilizes stereoselective zinc-mediated allylation, aldol coupling and ring-closing metathesis as key steps.
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## 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.
## 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 βFull Textβ option. The original article is trackable v
A new synthesis of (-)-rishitin (1) is reported, starting with chiral pool molecules. The crucial step is a stereo,selective vinyl radical eyelization, which gives a 10:1 ratio of 21 to 22.