Brønsted acid catalyzed asymmetric diels-alder reactions: Stereoselective construction of spiro[tetrahydrocarbazole-3,3'-oxindole] framework

Journal of Organic Chemistry

Volumn 80, Issue 6, 2015, Pages 3223-3232

  Wang, Yang ^a   Tu, Man Su ^a   Yin, Lei ^a   Sun, Meng ^a   Shi, Feng ^a  

^a JIANGSU NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; HYDROGEN BONDS; STEREOSELECTIVITY;

DIELS-ALDER REACTION; EFFICIENT STRATEGY; HIGH YIELD; METHYLENEINDOLINONES; OPTICAL PURITY; OXINDOLES; STEREOGENIC CENTERS; STEREOSELECTIVE CONSTRUCTION;

CHEMICAL REACTIONS;

BRONSTED ACID; INDOLE DERIVATIVE; OXINDOLE; PHOSPHORIC ACID DERIVATIVE; SPIRO[TETRAHYDROCARBAZOLE 3,3' OXINDOLE]; UNCLASSIFIED DRUG; PHOSPHORIC ACID; SPIRO COMPOUND; SPIRO(TETRAHYDROCARBAZOLE-3,3'-OXINDOLE);

ARTICLE; ASYMMETRIC CATALYSIS; CATALYST; CONTROLLED STUDY; DIASTEREOISOMER; DIELS ALDER REACTION; ENANTIOSELECTIVITY; HYDROGEN BOND; ISOMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STEREOSPECIFICITY; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; INDOLES; MOLECULAR STRUCTURE; PHOSPHORIC ACIDS; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84925374639     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.5b00198     Document Type: Article

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