Nickel-catalyzed Mizoroki-Heck reaction of aryl sulfonates and chlorides with electronically unbiased terminal olefins: High selectivity for branched products

Angewandte Chemie - International Edition

Volumn 53, Issue 7, 2014, Pages 1858-1861

  Tasker, Sarah Z ^a   Gutierrez, Alicia C ^a   Jamison, Timothy F ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

alkenes; Heck reaction; nickel; regioselectivity

Indexed keywords

ARYL ELECTROPHILES; BIDENTATE LIGANDS; COUNTERION EXCHANGES; HECK REACTIONS; HIGH SELECTIVITY; MIZOROKI-HECK REACTION; TERMINAL OLEFINS; TRIFLUOROMETHANESULFONATE;

CATALYSIS; CHLORINE COMPOUNDS; OLEFINS; REGIOSELECTIVITY; SULFUR COMPOUNDS;

NICKEL;

ALKENE; ARYLSULFONIC ACID DERIVATIVE; CHLORIDE; NICKEL;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; HECK REACTION; REGIOSELECTIVITY; STEREOISOMERISM; SYNTHESIS;

ALKENES; HECK REACTION; NICKEL; REGIOSELECTIVITY;

ALKENES; ARYLSULFONATES; CATALYSIS; CHLORIDES; MOLECULAR STRUCTURE; NICKEL; STEREOISOMERISM;

EID: 84893616766     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201308391     Document Type: Article

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