Highly diastereo- and enantioselective construction of a spiro[cyclopenta[b]indole-1,3’-oxindole] scaffold via catalytic asymmetric formal [3+2] cycloadditions

Chemical Communications

Volumn 50, Issue 100, 2014, Pages 15901-15904

  Tan, Wei ^a   Li, Xin ^a   Gong, Yu Xin ^a   Ge, Meng Di ^a   Shi, Feng ^a  

^a JIANGSU NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

3 INDOLEMETHANOL; 3 METHYL 2 VINYLINDOLE; CARBON; INDOLE DERIVATIVE; ISATIN; MOLECULAR SCAFFOLD; SPIRO[CYCLOPENTA[B]INDOLE 1,3' OXINDOLE]; UNCLASSIFIED DRUG; SPIRO COMPOUND;

ARTICLE; ASYMMETRIC CATALYSIS; CONTROLLED STUDY; CYCLOADDITION; DIASTEREOISOMER; ENANTIOSELECTIVITY; CATALYSIS; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; CYCLOADDITION REACTION; INDOLES; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84911917223     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c4cc07246d     Document Type: Article

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