SCOPUS 정보 검색 플랫폼

Volumn 19, Issue 18, 2013, Pages 5551-5556

3-isothiocyanato oxindoles serving as powerful and versatile precursors to structurally diverse dispirocyclic thiopyrrolidineoxindoles through a cascade Michael/cyclization process with amino-thiocarbamate catalysts

(5) Han, Wen Yong a,b Li, Shi Wu a,b Wu, Zhi Jun a Zhang, Xiao Mei a Yuan, Wei Cheng a

a CHENGDU INSTITUTE OF ORGANIC CHEMISTRY (China)

b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES (China)

Author keywords

asymmetric catalysis; cascade reactions; organocatalysis; oxindoles; stereoselectivity

Indexed keywords

ASYMMETRIC CATALYSIS; CASCADE REACTIONS; ORGANOCATALYSIS; OXINDOLES; QUANTITATIVE YIELDS; STEREOGENIC CENTERS;

CATALYSTS; REACTION KINETICS; STEREOSELECTIVITY;

CATALYSIS;

FUSED HETEROCYCLIC RINGS; INDOLE DERIVATIVE; ISOTHIOCYANIC ACID DERIVATIVE; OXINDOLE; SPIRO COMPOUND; THIOCARBAMIC ACID DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; CYCLIZATION; HETEROCYCLIC COMPOUNDS WITH 4 OR MORE RINGS; INDOLES; ISOTHIOCYANATES; MOLECULAR STRUCTURE; SPIRO COMPOUNDS; STEREOISOMERISM; THIOCARBAMATES;

EID: 84876896788 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.201300206 Document Type: Article

Times cited : (110)

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