Iodine(III)-mediated halogenations of acyclic monoterpenoids

Five different halofunctionalizations of acyclic monoterpenoids were performed using a combination of a hypervalent iodine(III) reagent and a halide salt. In this manner, the dibromination, the bromo(trifluoro)acetoxylation, the bromohydroxylation, the iodo(trifluoro)acetoxylation or the ene-type ch...

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Detalles Bibliográficos
Autores principales: Peilleron, Laure, Grayfer, Tatyana D, Dubois, Joëlle, Dodd, Robert H, Cariou, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009204/
https://www.ncbi.nlm.nih.gov/pubmed/29977382
http://dx.doi.org/10.3762/bjoc.14.96

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009204/
https://www.ncbi.nlm.nih.gov/pubmed/29977382
http://dx.doi.org/10.3762/bjoc.14.96

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