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Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor

A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps.

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Dettagli Bibliografici
Pubblicato in:Beilstein J Org Chem
Autori principali: Saha, Nemai, Chattopadhyay, Shital K
Natura: Artigo
Lingua:Inglês
Pubblicazione: Beilstein-Institut 2014
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4311665/
https://ncbi.nlm.nih.gov/pubmed/25670979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.10.327
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