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Recent advances in palladium-catalyzed (hetero)annulation of C[double bond, length as m-dash]C bonds with ambiphilic organo(pseudo)halides.
Ni, Hui-Qi; Cooper, Phillippa; Engle, Keary M.
Affiliation
  • Ni HQ; The Scripps Research Institute, Department of Chemistry, 10550 N. Torrey Pines Rd, La Jolla, California, USA. keary@scripps.edu.
  • Cooper P; The Scripps Research Institute, Department of Chemistry, 10550 N. Torrey Pines Rd, La Jolla, California, USA. keary@scripps.edu.
  • Engle KM; The Scripps Research Institute, Department of Chemistry, 10550 N. Torrey Pines Rd, La Jolla, California, USA. keary@scripps.edu.
Chem Commun (Camb) ; 57(62): 7610-7624, 2021 Aug 03.
Article in En | MEDLINE | ID: mdl-34278397
Palladium has proven to be effective in catalyzing the (hetero)annulation of C[double bond, length as m-dash]C bonds with ambiphilic organo(pseudo)halides. Through the employment of appropriate ambiphilic coupling partners, efficient annulation of a variety of allenes, 1,3-dienes, strained alkenes, styrenes, and other C[double bond, length as m-dash]C bond variants can be achieved to provide direct access to numerous useful hetero- and carbocyclic scaffolds. In this Feature Article, we summarize palladium-catalyzed (hetero)annulation methods reported since 2005 (spanning just over 15 years) and discuss outstanding challenges in this area of study.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2021 Type: Article Affiliation country: United States