Trans -diborylation of alkynes: Pseudo -intramolecular strategy utilizing a propargylic alcohol unit

Journal of the American Chemical Society

Volumn 136, Issue 24, 2014, Pages 8532-8535

  Nagashima, Yuki ^a   Hirano, Keiichi ^a   Takita, Ryo ^b   Uchiyama, Masanobu ^a,b  

^a UNIVERSITY OF TOKYO   (Japan)

^b Elements Chemistry Laboratory   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ENERGY; ALCOHOLS;

ALKOXIDES; BOND ACTIVATION; BOND FORMATION; COMPUTATIONAL ANALYSIS; FUNCTIONALIZED; PROPARGYL ALCOHOL; PROPARGYLIC ALCOHOLS; REACTION ANALYSIS;

HYDROCARBONS;

ALCOHOL; ALKYNE DERIVATIVE; BORONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VINYLDIBORONATE DERIVATIVE; ALKYNE; PROPANOL; PROPARGYL ALCOHOL;

ARTICLE; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIBORYLATION; CHEMISTRY; SYNTHESIS;

ALKYNES; BORONIC ACIDS; MOLECULAR STRUCTURE; PROPANOLS;

EID: 84902665565     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja5036754     Document Type: Article

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