Diastereoselectivity on Intramolecular Alder‐ene Reaction of 1,6‐Dienes

A detailed computational study of the intramolecular Alder‐ene reaction of different 1,6‐dienes at M06‐2X(PCM)/TZ2P level of theory has been performed. We want to understand the influence of enophile‐geminal substitution pattern in the cis : trans selectivity of the cyclization process. Our analysis...

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Detalles Bibliográficos
Autor principal: de Cózar, Abel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087545/
https://www.ncbi.nlm.nih.gov/pubmed/35942565
http://dx.doi.org/10.1002/cphc.202200377

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087545/
https://www.ncbi.nlm.nih.gov/pubmed/35942565
http://dx.doi.org/10.1002/cphc.202200377

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