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Volumn 75, Issue 17, 2010, Pages 6027-6030

Direct asymmetric hydrogenation of 2-oxo-4-arylbut-3-enoic acids

Author keywords

[No Author keywords available]

Indexed keywords

ACE INHIBITORS; ASYMMETRIC HYDROGENATION; CHIRAL LIGAND; HYDROGENATION PROCESS; REACTION CONDITIONS; RU CATALYSTS;

EID: 77956140066     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101084t     Document Type: Article
Times cited : (29)

References (86)
  • 70
    • 77956165973 scopus 로고    scopus 로고
    • After reviewing our manuscript, one reviewer kindly suggested we do more experiments to make it clear whether the counterion or the aqueous reaction condition plays a more important role in achieving high enantioselectivity
    • After reviewing our manuscript, one reviewer kindly suggested we do more experiments to make it clear whether the counterion or the aqueous reaction condition plays a more important role in achieving high enantioselectivity.
  • 71
    • 77956159126 scopus 로고    scopus 로고
    • If the hydrogenation was terminated after 5 h, the conversion is 25%. The product 2a (S) was 35.4% ee, and the unreacted starting material 3a (R) was 19.0% ee
    • If the hydrogenation was terminated after 5 h, the conversion is 25%. The product 2a (S) was 35.4% ee, and the unreacted starting material 3a (R) was 19.0% ee.
  • 85
    • 77956161720 scopus 로고    scopus 로고
    • (BASF AG, Germany) PCT Int. Appl. WO2006040096
    • Jaekel, C.; Paciello, R. (BASF AG, Germany) PCT Int. Appl. WO2006040096, 2006.
    • (2006)
    • Jaekel, C.1    Paciello, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.