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An Enantioselective Approach to the Hetisine Alkaloids. Synthesis of the 3-Methyl-1-aza-tricyclo[5.2.1.0(3,8)]decane Core via Intramolecular Dipolar Cycloaddition

An efficient, enantioselective approach to the hetisine class of the C(20)-diterpenoid alkaloids is described. The strategy involves an intramolecular oxidopyridinium dipolar cycloaddition as the key transformation, in which simultaneous formation of the C5-C6 and C10-C20 bonds in the 3-methyl-1-aza...

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Autori principali: Peese, Kevin M., Gin, David Y.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2005
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2593868/
https://ncbi.nlm.nih.gov/pubmed/16018651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol051184v
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