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Simple Sulfinate Synthesis Enables C–H Trifluoromethylcyclopropanation

A simple method to convert readily available carboxylic acids into sulfinate salts employing an interrupted Barton decarboxylation reaction is reported. A medicinally oriented panel of ten new sulfinate reagents was created using this method, including a key trifluoromethylcyclopropanation reagent T...

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Detalhes bibliográficos
Main Authors: Gianatassio, Ryan, Kawamura, Shuhei, Eprile, Cecil L, Foo, Klement, Ge, Jason, Burns, Aaron C., Collins, Michael R., Baran, Phil S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4186797/
https://ncbi.nlm.nih.gov/pubmed/25088979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.201406622
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