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Volumn 64, Issue 37, 2008, Pages 8700-8708

Preparation of pyridinyl aryl methanol derivatives by enantioselective hydrogenation of ketones using chiral Ru(diphosphine)(diamine) complexes. Attribution of their absolute configuration by 1H NMR spectroscopy using Mosher's reagent

Author keywords

Enantioselective hydrogenation; Mosher's ester; Pyridinyl aryl methanol; Ruthenium catalysts

Indexed keywords

CYCLOHEXANE DERIVATIVE; FLUORENE DERIVATIVE; SPIROCYCLOHEXANE;

EID: 48049123674     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.06.104     Document Type: Article
Times cited : (24)

References (43)
  • 1
    • 48049116259 scopus 로고    scopus 로고
    • Selected examples:
    • Selected examples:
  • 34
    • 22144467710 scopus 로고    scopus 로고
    • The assignment of the absolute configuration of some pyridyl aryl carbinols based on NMR analyses of (R) and (S)-MPA esters has been previously reported but no correlation between the nature of the prevalent enantiomer and the conditions of the asymmetric hydrogenation of the corresponding ketone is available. See:
    • The assignment of the absolute configuration of some pyridyl aryl carbinols based on NMR analyses of (R) and (S)-MPA esters has been previously reported but no correlation between the nature of the prevalent enantiomer and the conditions of the asymmetric hydrogenation of the corresponding ketone is available. See:. Chen C.-y., Reamer R.A., Roy A., and Chilenski J.R. Tetrahedron Lett. 46 (2005) 5593-5596
    • (2005) Tetrahedron Lett. , vol.46 , pp. 5593-5596
    • Chen, C.-y.1    Reamer, R.A.2    Roy, A.3    Chilenski, J.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.