Facile enantiospecific syntheses of oxabicyclo[4.4.0]decene-diones from carvone via mild Lewis acid mediated lactonizations
By: Adusumilli, Srikrishna.
Contributor(s): Satyanarayana, Gedu.
Publisher: New Delhi CSIR 2019Edition: Vol.58(B), March.Description: 362-370p.Subject(s): GENERAL CHEMISTRYOnline resources: Click here In: Indian journal of chemistry (Section B)Summary: An efficient and concise enantiospecific syntheses of oxabicyclo[4.4.0]decene-diones have been accomplished starting from carvone. This strategy is a chiron based approach by making use of mild Lewis acid mediated intramolecular lactonization as key step for the formation of fused bicyclic lactones. Notably, these bicyclic lactones constitute bicyclic carbon framework of diterpene natural products.Item type | Current location | Call number | Status | Date due | Barcode | Item holds |
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Articles Abstract Database | School of Pharmacy Archieval Section | Not for loan | 2022-0311 |
Total holds: 0
An efficient and concise enantiospecific syntheses of oxabicyclo[4.4.0]decene-diones have been accomplished starting from carvone. This strategy is a chiron based approach by making use of mild Lewis acid mediated intramolecular lactonization as key step for the formation of fused bicyclic lactones. Notably, these bicyclic lactones constitute bicyclic carbon framework of diterpene natural products.
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