Synthesis of methyl (1R,2S)-α,α-dimethyl-3-oxo-2-pentylcyclopentaneacetate. A model procedure for the preparation of chiral jasmonoids and prostaglandins
✍ Scribed by A García Martínez; E Teso Vilar; A García Fraile; S de la Moya Cerero; P Martínez Ruiz; P.P García Álvarez
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 216 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0957-4166
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✦ Synopsis
An expeditious procedure for the enantiospecific preparation of the trans-2,3disubstituted cyclopentanone moiety starting from natural 2-norbornanones is described. New reaction conditions for the reaction of sterically hindered ketones with triflic anhydride, as well as for the S-O cleavage of bridgehead triflates have been developed.
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