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Volumn 21, Issue 3, 2015, Pages 1004-1008

Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction

(4) Zou, Liang Hua a Philipps, Arne R a Raabe, Gerhard a Enders, Dieter a

a RWTH AACHEN UNIVERSITY (Germany)

Author keywords

Asymmetric synthesis; Cyclopentanes; Domino reactions; Organocatalysis; Oxindoles

Indexed keywords

FUNCTIONAL GROUPS; REACTION KINETICS;

ASYMMETRIC SYNTHESIS; CYCLOPENTANES; DOMINO REACTIONS; ORGANOCATALYSIS; OXINDOLES;

SYNTHESIS (CHEMICAL);

CYCLOPENTANE DERIVATIVE; INDOLE DERIVATIVE; OXINDOLE;

CATALYSIS; CHEMISTRY; CONFORMATION; CYCLIZATION; STEREOISOMERISM; X RAY CRYSTALLOGRAPHY;

CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; CYCLOPENTANES; INDOLES; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 84920854506 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.201406047 Document Type: Article

Times cited : (37)

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- According to the Björkling group, some S-configured oxindole derivatives possess potential antitumor activity, while the racemic compounds show complete tumor regression. The enantiomers were separated by chiral stationary-phase chromatography.

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