An organocatalytic domino Michael-alkylation reaction: Highly enantioselective construction of spiro-cyclopentanoneoxindoles and tetronic acid scaffolds

Chemical Communications

Volumn 50, Issue 93, 2014, Pages 14601-14604

  Zhou, Jing ^a,b   Wang, Qi Lin ^a,b   Peng, Lin ^a   Tian, Fang ^a   Xu, Xiao Ying ^a   Wang, Li Xin ^a  

^a INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

[No Author keywords available]

Indexed keywords

FURAN DERIVATIVE; INDOLE DERIVATIVE; SPIRO COMPOUND; TETRONIC ACID; MOLECULAR SCAFFOLD; OXINDOLE; SPIRO CYCLOPENTANONEOXINDOLE; TETRONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; ARTICLE; ASYMMETRIC CATALYSIS; CATALYST; CONTROLLED STUDY; CYCLIZATION; DIASTEREOISOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MICHAEL ADDITION; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY;

ALKYLATION; CATALYSIS; FURANS; INDOLES; MOLECULAR STRUCTURE; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84908676073     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c4cc05207b     Document Type: Article

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