Correlation between functionality preference of ru carbenes and exo / endo product selectivity for clarifying the mechanism of ring-closing enyne metathesis

Journal of Organic Chemistry

Volumn 78, Issue 17, 2013, Pages 8242-8249

  Lee, Ok Suk ^a   Kim, Kyung Hwan ^b,c   Kim, Jinwoo ^b   Kwon, Kuktae ^b   Ok, Taedong ^d   Ihee, Hyotcherl ^b,c   Lee, Hee Yoon ^b   Sohn, Jeong Hun ^a  

^a Chungnam National University   (South Korea)

^b Korea Advanced Institute of Science and Technology (KAIST)   (South Korea)

^c Institute for Basic Science   (South Korea)

^d Yonsei University College of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ENYNE METATHESIS; FLUORESCENCE QUENCHING; GOOD CORRELATIONS; METATHESIS REACTIONS; MULTIPLE BONDS; PRODUCT SELECTIVITIES; REACTION PATHWAYS; SUBSTITUTION PATTERNS;

CHEMISTRY; ORGANIC COMPOUNDS;

HYDROCARBONS;

ALKENE; ALKYNE; CARBENE; ENYNE; FUNCTIONAL GROUP; RUTHENIUM; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CHEMICAL STRUCTURE; CORRELATION ANALYSIS; FLUORESCENCE RESONANCE ENERGY TRANSFER; RING CLOSING METATHESIS;

ALKENES; ALKYNES; CATALYSIS; CYCLIZATION; FLUORESCENCE; LIGANDS; METHANE; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; RUTHENIUM; TIME FACTORS;

EID: 84883748662     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo401420f     Document Type: Article

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