The intramolecular ene reaction of the 1,6-diene on a bicyclo[3.2.1]octane framework proceeds in a highly diastereoselective manner to form a trisubstituted pyrrolidine on the pyran ring in excellent yield. Its stereochemistry has been determined unambiguously by converting it into the known compoun
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Intramolecular diyl trapping reactions en route to the bicyclo [3.2.1] framework; an approach to aphidicolin
β Scribed by Wei Zhong; R. Daniel Little
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 530 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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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 βFull Textβ option. The original article is trackable v
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