Highly efficient hydrogen-bonding catalysis of the diels-alder reaction of 3-vinylindoles and methyleneindolinones provides carbazolespirooxindole skeletons

Journal of the American Chemical Society

Volumn 133, Issue 32, 2011, Pages 12354-12357

  Tan, Bin ^a   Hernández Torres, Gloria ^a,b   Barbas, Carlos F ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

BISTHIOUREA; DIELS-ALDER REACTION; DIVERSITY-ORIENTED SYNTHESIS; ENANTIOPURITY; H-BONDING; HYDROGEN BONDINGS; OPERATIONAL PROCEDURES; ORGANOCATALYSTS; STRUCTURAL DIVERSITY;

CATALYSIS;

BISTHIOUREA; CARBAZOLE DERIVATIVE; CARBAZOLESPIROOXINDOLE; HYDROGEN; INDOLE DERIVATIVE; SOLVENT; THIOUREA DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC CATALYSIS; CATALYST; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; DIELS ALDER REACTION; ENANTIOSELECTIVITY; HYDROGEN BOND; STEREOCHEMISTRY; SYNTHESIS;

CATALYSIS; HYDROGEN BONDING; INDOLES; STEREOISOMERISM; THIOUREA;

EID: 80051594488     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja203812h     Document Type: Article

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