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Publikováno v:
ChemInform. 36
The enantioselective total synthesis of the actin-targeting metabolite (−)-microcarpalide is described. Key steps include ring-closing metathesis (RCM) for the final construction of the 10-membered lactone framework and stereoselective homologation
The enantioselective total synthesis of the actin-targeting metabolite (−)-microcarpalide is described. Key steps include ring-closing metathesis (RCM) for the final construction of the 10-membered lactone framework and stereoselective homologation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfd7577d292997b82fd9413698d25dd9
https://hdl.handle.net/11380/307116
https://hdl.handle.net/11380/307116