SCOPUS 정보 검색 플랫폼

Volumn 8, Issue 8, 2013, Pages 1768-1771

Catalytic asymmetric synthesis of spirooxindoles via addition of isothiocyanato oxindoles to aldehydes under dinuclear nickel schiff base catalysis

(3) Kato, Shota a Kanai, Motomu a Matsunaga, Shigeki a,b

a UNIVERSITY OF TOKYO (Japan)

b JAPAN SCIENCE AND TECHNOLOGY AGENCY (Japan)

Author keywords

asymmetric catalysis; asymmetric synthesis; oxindole; salen; spiro compounds

Indexed keywords

ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; OXINDOLE; SALEN; SPIRO COMPOUNDS;

CATALYSIS; CATALYSTS; FUNCTIONAL GROUPS;

NICKEL;

ALDEHYDE; INDOLE DERIVATIVE; ISOTHIOCYANIC ACID DERIVATIVE; NICKEL; OXINDOLE; SCHIFF BASE; SPIRO COMPOUND;

ARTICLE; ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; CATALYSIS; CHEMISTRY; CONFORMATION; SALEN; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; OXINDOLE; SALEN; SPIRO COMPOUNDS;

ALDEHYDES; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; INDOLES; ISOTHIOCYANATES; MOLECULAR CONFORMATION; NICKEL; SCHIFF BASES; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84881135316 PISSN: 18614728 EISSN: 1861471X Source Type: Journal
DOI: 10.1002/asia.201300251 Document Type: Conference Paper

Times cited : (51)

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- CCDC 925955 (4-bromobenzoylated 4 aa) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.
- These Data Can Be Obtained Free of Charge from the Cambridge Crystallographic Data Centre Via

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- In this study, only isothiocyanato-oxindoles bearing a substituent at either 5 or 6-position were utilized due to limitations in availability. Full scope and limitations of 4- and/or 7-substituted isothiocyanato-oxindoles will be reported in due course.
- Full Scope and Limitations of 4- And/or 7-substituted Isothiocyanato-oxindoles Will Be Reported in Due Course

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