Stereoselective Synthesis of Methyl trans-Chrysanthemate and Related Derivatives. -The title esters (III) and (IV) are prepared by a novel type of cyclopropane formation. It is noteworthy that the earlier reported thionyl chloride-triethylamine method for the cyclization step is not successful. In
β¦ LIBER β¦
A convenient regio- and stereospecific synthesis of 2H-labelled methyl trans-chrysanthemate
β Scribed by Manoucher Saljoughian
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- French
- Weight
- 112 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0022-2135
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