Computation and experiment reveal that the ring-rearrangement metathesis of himbert cycloadducts can be subject to kinetic or thermodynamic control

Journal of the American Chemical Society

Volumn 135, Issue 46, 2013, Pages 17585-17594

  Lam, Jonathan K ^a   Pham, Hung V ^b   Houk, K N ^b   Vanderwal, Christopher D ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPUTATIONAL INVESTIGATION; DIASTEREO-SELECTIVITY; KINETIC CONTROL; REACTION PATHWAYS; RELATED SYSTEMS; RING CLOSING METATHESIS; RING OPENING METATHESIS; THERMODYNAMIC CONTROL;

CHEMISTRY; SYNTHESIS (CHEMICAL);

SUBSTRATES;

POLYCYCLIC AROMATIC HYDROCARBON;

ARTICLE; CYCLOADDITION; ENERGY TRANSFER; KINETICS; REACTION ANALYSIS; RING CLOSING METATHESIS; STEREOCHEMISTRY; THERMODYNAMICS;

CYCLIZATION; KINETICS; MOLECULAR STRUCTURE; QUANTUM THEORY; STEREOISOMERISM; THERMODYNAMICS;

EID: 84888345070     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja409618p     Document Type: Article

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