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Vinylidenation of Organoboronic Esters Enabled by a Pd-Catalyzed Metallate Shift.

Organoboron ‘ate’ complexes undergo a net vinyl insertion reaction to give 1,1-disubstituted alkenyl boronic esters when treated with stoichiometric allyl acetate and a palladium catalyst. Reactions that employ vinyllithium afforded good to excellent yields after one hour, while reactions that emplo...

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Detalhes bibliográficos
Publicado no:Angew Chem Int Ed Engl
Main Authors: Aparece, Mark D., Gao, Chenpeng, Lovinger, Gabriel J., Morken, James P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6414219/
https://ncbi.nlm.nih.gov/pubmed/30444946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.201811782
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