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Volumn 65, Issue 45, 2009, Pages 9481-9486

New organocatalysts for the asymmetric reduction of imines with trichlorosilane

Author keywords

Asymmetric catalysis; Enantioselective reduction; Hydrosilylation; Lewis basic catalysts; Organocatalysis; Trichlorosilane

Indexed keywords

3,5 DI (2' TOLYL)ANILINE; 3,5 DI (2' TOLYL)NITROBENZENE; 3,5 DIBROMONITROBENZENE; 3,5 DIPHENYLANILINE; 3,5 DIPHENYLNITROBENZENE; AMIDE; AROMATIC COMPOUND; FORMAMIDE; IMINE; KETIMINE DERIVATIVE; LEWIS BASE; N METHYL VALINE; SILANE DERIVATIVE; TOLUENE; TRICHLOROSILANE; UNCLASSIFIED DRUG; VALINE;

EID: 70349971153     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.08.048     Document Type: Article
Times cited : (36)

References (102)
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    • For an overview, see:
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    • For the kinetic resolution using transfer hydrogenation combined with an ezymatic reaction, see:
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    • 2H, Ru), see:
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    • For a different approach, employing a chiral Brønsted acid as catalyst and Hantzsch dihydropyridine as a reducing agent, see the following
    • For a different approach, employing a chiral Brønsted acid as catalyst and Hantzsch dihydropyridine as a reducing agent, see the following:
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    • 3SiH, catalyzed by metal-free Lewis bases, see:
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    • note
    • 13 However, in the coupling reaction, the dibromide should act as an electrophile, which is a role better suited to the electron-poor nitro derivative 6 than to its amino analogue.
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    • See Ref. 11b and the following:
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    • note
    • 11f,g


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.