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Volumn 3, Issue 7, 2008, Pages 1104-1110

Synthesis of enantiomerically pure 1,2,3,4-tetrahydro-β-carbolines and N-acyl-1-aryl ethylamines by rhodium-catalyzed hydrogenation

Author keywords

Asymmetric hydrogenation; Enamides; Homogeneous catalysis; Hydro carbolines; Phosphane ligands

Indexed keywords

CARBOLINE DERIVATIVE; ETHYLAMINE; LIGAND; RHODIUM;

EID: 49149112782     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200800111     Document Type: Article
Times cited : (24)

References (85)
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    • All hydrogenation reactions were carried out in an eight-fold parallel reactor array with a reactor of 3.0 mL (Institute of Automation IAT, Richard Wagner Str. 31/H. 8, 18119 Rostock-Warnemünde, Germany
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    • In the case of tBu-Binepine, methanol was used as the solvent because the catalyst displayed higher enantioselectivity with methanol than with dichloromethane.
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    • (E/Z)-1-(1-(2-Phenylethylidene)-3,4-dihydro-1H-pyrido[3, 4-b]indol-2(9H)-yl)ethanone.
    • (E/Z)-1-(1-(2-Phenylethylidene)-3,4-dihydro-1H-pyrido[3, 4-b]indol-2(9H)-yl)ethanone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.