Structurally and stereochemically diverse tetrahydropyran synthesis through oxidative C-H bond activation

Angewandte Chemie - International Edition

Volumn 49, Issue 17, 2010, Pages 3069-3072

  Liu, Lei ^a   Floreancig, Paul E ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

Combinatorial synthesis; Diastereoselectivity; Drosilylation; Molecular diversity; Oxidation

Indexed keywords

BENZOQUINONES; C-H BOND; CH-BOND ACTIVATION; CHEMICAL EQUATIONS; COMBINATORIAL SYNTHESIS; DIASTEREO-SELECTIVITY; DIVERSITY-ORIENTED SYNTHESIS; DROSILYLATION; FUNCTIONALIZATIONS; INTERCONVERSIONS; MOLECULAR DIVERSITY; TETRAHYDROPYRAN; VINYL SILANE;

CHEMICAL BONDS; DOPING (ADDITIVES); ETHERS; FUNCTIONAL GROUPS; OXIDATION; STEREOSELECTIVITY;

SYNTHESIS (CHEMICAL);

PYRAN DERIVATIVE;

ARTICLE; CATALYSIS; CHEMISTRY; COMBINATORIAL CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; OXIDATION-REDUCTION; PYRANS; STEREOISOMERISM;

EID: 77951165523     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201000033     Document Type: Article

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