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Volumn 16, Issue 32, 2010, Pages 9763-9766

Organocatalytic asymmetric synthesis of trans-1,3-disubstituted tetrahydroisoquinolines via a reductive amination/aza-michael sequence

Author keywords

Asymmetric synthesis; Michael addition; Organocatalysis; Phosphoric acid; Reductive amination

Indexed keywords

ASYMMETRIC SYNTHESIS; BENZOTHIAZOLINE; ENANTIOMERIC EXCESS; MICHAEL ADDITION; ORGANOCATALYSIS; ORGANOCATALYTIC; POTASSIUM TERT-BUTOXIDE; REDUCTIVE AMINATION; STEREO-SELECTIVE; TETRAHYDROISOQUINOLINES;

EID: 77955860588     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001623     Document Type: Article
Times cited : (75)

References (65)
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    • For example the corresponding ethyl ketone of 7e could be reduced with 92% ee but only 23% yield was obtained.
    • For example the corresponding ethyl ketone of 7e could be reduced with 92% ee but only 23% yield was obtained.
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    • CCDC-773769 contains the supplementary crystallographic data for this paper (excluding structure factors). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-773769 contains the supplementary crystallographic data for this paper (excluding structure factors). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.
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    • See the Supporting Information for details.
    • See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.