SCOPUS 정보 검색 플랫폼

Volumn 18, Issue 26, 2012, Pages 8008-8012

Asymmetric supramolecular catalysis: A bio-inspired tool for the high asymmetric induction in the enamine-based Michael reactions

(3) Ramachary, Dhevalapally B a Sakthidevi, Rajasekar a Shruthi, Kodambahalli S a

a UNIVERSITY OF HYDERABAD (India)

Author keywords

asymmetric catalysis; Michael addition; organocatalysis; supramolecular chemistry; synthetic methods

Indexed keywords

ABSOLUTE STEREOCHEMISTRY; ASYMMETRIC CATALYSIS; ASYMMETRIC INDUCTION; BIO-INSPIRED; CHROMENES; CYCLOHEXANONES; ENANTIOMERIC EXCESS; HIGH YIELD; L-PROLINE; LACTOLS; MICHAEL ADDITIONS; MICHAEL REACTIONS; ORGANOCATALYSIS; REDUCTIVE ETHERIFICATION; SUPRAMOLECULAR ASSEMBLIES; SUPRAMOLECULAR CATALYSIS; SYNTHETIC METHODS;

ADDITION REACTIONS; AMINO ACIDS; CATALYSIS; ENANTIOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHENOLS; REACTION KINETICS; STEREOCHEMISTRY; SUPRAMOLECULAR CHEMISTRY; THIOUREAS;

ENANTIOSELECTIVITY;

BIPHENYL DERIVATIVE; CYCLOHEXANONE DERIVATIVE; DRUG DERIVATIVE; ENAMINE; IMIDAZOLE DERIVATIVE; PHENOL DERIVATIVE; PROLINE; THIOUREA; XANTHENE DERIVATIVE;

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

BIPHENYL COMPOUNDS; CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; CYCLOHEXANONES; IMIDAZOLES; MOLECULAR STRUCTURE; PHENOLS; PROLINE; STEREOISOMERISM; THIOUREA; XANTHENES;

EID: 84863795889 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.201200962 Document Type: Article

Times cited : (62)

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