The direct oxidative diene cyclization and related reactions in natural product synthesis

The direct oxidative cyclization of 1,5-dienes is a valuable synthetic method for the (dia)stereoselective preparation of substituted tetrahydrofurans. Closely related reactions start from 5,6-dihydroxy or 5-hydroxyalkenes to generate similar products in a mechanistically analogous manner. After a b...

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Detalles Bibliográficos
Autores principales: Adrian, Juliane, Gross, Leona J, Stark, Christian B W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082725/
https://www.ncbi.nlm.nih.gov/pubmed/27829917
http://dx.doi.org/10.3762/bjoc.12.200

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082725/
https://www.ncbi.nlm.nih.gov/pubmed/27829917
http://dx.doi.org/10.3762/bjoc.12.200

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