Comparison of arylboron-based nucleophiles in Ni-catalyzed Suzuki-Miyaura cross-coupling with aryl mesylates and sulfamates

Journal of Organic Chemistry

Volumn 77, Issue 14, 2012, Pages 5956-5964

  Zhang, Na ^a   Hoffman, David J ^a   Gutsche, Nicholas ^a   Gupta, Jayesh ^a   Percec, Virgil ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARYLBORONIC ACIDS; BORONATE; BORONIC ACID; ELECTROPHILES; MESYLATES; PINACOLS; PRESENCE OF WATER; SULFAMATES; SUZUKI-MIYAURA CROSS-COUPLING; SUZUKI-MIYAURA CROSS-COUPLING REACTION;

BORON; NUCLEOPHILES; POTASSIUM;

CATALYSIS;

4 METHOXYPHENYL NEOPENTYLGLYCOLBORONATE; 4 METHOXYPHENYL PINACOLBORONATE; BORON; BORONIC ACID DERIVATIVE; MESYLIC ACID; METHYL 4 [(METHYLSULFONYL)OXY]BENZOATE; NEOPENTYLGLYCOLBORONATE; NICKEL; NUCLEOPHILE; PINACOL BORONATE; POTASSIUM TRIFLUOROBORATE; SULFAMIC ACID; SULFUR ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; STOICHIOMETRY; SUZUKI REACTION; SYNTHESIS;

BENZENE DERIVATIVES; BORONIC ACIDS; CATALYSIS; MESYLATES; MOLECULAR STRUCTURE; NICKEL; ORGANOMETALLIC COMPOUNDS; SULFONIC ACIDS;

EID: 84864060866     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300547v     Document Type: Article

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