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Volumn 17, Issue 4, 2006, Pages 521-535

Catalytic asymmetric hydrogenation of indoles using a rhodium complex with a chiral bisphosphine ligand PhTRAP

Author keywords

[No Author keywords available]

Indexed keywords

CHELATE; INDOLE DERIVATIVE; PHOSPHINE DERIVATIVE; RHODIUM COMPLEX; TRANSITION ELEMENT;

EID: 33645913553     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.01.016     Document Type: Article
Times cited : (109)

References (44)
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    • Recent reviews:
    • Recent reviews:. Tang W., and Zhang X. Chem. Rev. 103 (2003) 3029-3069
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    • Tang, W.1    Zhang, X.2
  • 5
    • 0001134614 scopus 로고    scopus 로고
    • Hydrogenations of aromatic compounds with a chiral auxiliary have been reported, but gave the products in low yields and/or stereoselectivities, see:
    • Hydrogenations of aromatic compounds with a chiral auxiliary have been reported, but gave the products in low yields and/or stereoselectivities, see:. Besson M., Blanc B., Champelet M., Gallezot P., Nasar K., and Pinel C. J. Catal. 170 (1997) 254-264
    • (1997) J. Catal. , vol.170 , pp. 254-264
    • Besson, M.1    Blanc, B.2    Champelet, M.3    Gallezot, P.4    Nasar, K.5    Pinel, C.6
  • 15
    • 4344711567 scopus 로고    scopus 로고
    • Recently, Glorius reported the highly stereoselective hydrogenation of pyridines modified with a chiral oxazolidinone, see:
    • Recently, Glorius reported the highly stereoselective hydrogenation of pyridines modified with a chiral oxazolidinone, see:. Glorius F., Spielkamp N., Holle S., Goddard R., and Lehmann C.W. Angew. Chem., Int. Ed. 43 (2004) 2850-2852
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 2850-2852
    • Glorius, F.1    Spielkamp, N.2    Holle, S.3    Goddard, R.4    Lehmann, C.W.5
  • 18
    • 0003787433 scopus 로고    scopus 로고
    • Barton D., Nakanish K., and Meth-Cohn O. (Eds), Elsevier, Oxford
    • In: Barton D., Nakanish K., and Meth-Cohn O. (Eds). Comprehensive Natural Products Chemistry Vols. 1-9 (1999), Elsevier, Oxford
    • (1999) Comprehensive Natural Products Chemistry , vol.1-9
  • 30
    • 0345561665 scopus 로고    scopus 로고
    • Catalytic asymmetric hydrogenations of pyridines and furans have been reported but were low enantioselective, see:
    • Catalytic asymmetric hydrogenations of pyridines and furans have been reported but were low enantioselective, see:. Blaser H.-U., Höning H., Studer M., and Wedemeyer-Exl C. J. Mol. Catal. A: Chem. 139 (1999) 253-257
    • (1999) J. Mol. Catal. A: Chem. , vol.139 , pp. 253-257
    • Blaser, H.-U.1    Höning, H.2    Studer, M.3    Wedemeyer-Exl, C.4
  • 36
    • 33645912516 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess of 3-methylindoline was determined by chiral HPLC analysis of its acetamido derivative, which was prepared by the treatment with acetic anhydride.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.