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Volumn 130, Issue 3, 2008, Pages 808-809

Erratum: Catalytic asymmetric hydrogenation of 2,3,5-trisubstituted pyrroles (Journal of the American Chemical Society (2008) 130 (808-809) DOI: 10.1021/ja7102422);Catalytic asymmetric hydrogenation of 2,3,5-trisubstituted pyrroles

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE; LIGAND; METAL COMPLEX; PHOSPHINE DERIVATIVE; PYRROLE DERIVATIVE; PYRROLIDINE DERIVATIVE; RHODIUM COMPLEX; RUTHENIUM COMPLEX;

EID: 38349135761     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja2036332     Document Type: Erratum
Times cited : (122)

References (26)
  • 10
    • 0041825591 scopus 로고    scopus 로고
    • Representative examples: (a) Wang, W.-B.; Lu, S.-M.; Yang, P.-Y.; Han, X.-W.; Zhou, Y.-G. J. Am. Chem. Soc. 2003, 125, 10536-10537.
    • Representative examples: (a) Wang, W.-B.; Lu, S.-M.; Yang, P.-Y.; Han, X.-W.; Zhou, Y.-G. J. Am. Chem. Soc. 2003, 125, 10536-10537.
  • 14
    • 33746269442 scopus 로고    scopus 로고
    • High enantioselectivity was achieved in the reduction of quinolines with organocatalysis; see
    • High enantioselectivity was achieved in the reduction of quinolines with organocatalysis; see: Rueping, M.; Antonchick, A. P.; Theissmann, T. Angew. Chem., Int. Ed. 2006, 45, 3683-3686.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 3683-3686
    • Rueping, M.1    Antonchick, A.P.2    Theissmann, T.3
  • 16
    • 34250765230 scopus 로고    scopus 로고
    • Very recently, high enantioselectivity has been reported in the organocatalytic transfer hydrogenation of pyridines; see
    • Very recently, high enantioselectivity has been reported in the organocatalytic transfer hydrogenation of pyridines; see: Rueping, M.; Antonchick, A. P. Angew. Chem., Int. Ed. 2007, 46, 4562-4565.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 4562-4565
    • Rueping, M.1    Antonchick, A.P.2
  • 17
    • 4344711567 scopus 로고    scopus 로고
    • Highly stereoselective hydrogenation of pyridines modified with a chiral oxazolidinone with heterogeneous catalysis has been reported; see: Glorius, F, Spielkamp, N, Holle, S, Goddard, R, Lehmann, C. W. Angew. Chem, Int. Ed. 2004, 43, 2850-2852
    • Highly stereoselective hydrogenation of pyridines modified with a chiral oxazolidinone with heterogeneous catalysis has been reported; see: Glorius, F.; Spielkamp, N.; Holle, S.; Goddard, R.; Lehmann, C. W. Angew. Chem., Int. Ed. 2004, 43, 2850-2852.
  • 20
    • 0343289081 scopus 로고    scopus 로고
    • Highly stereoselective hydrogenation of a pyrrole modified with chiral auxiliary had been reported; see: Hada, V, Tungler, A, Szepesy, L. Appl. Catal. A 2001, 210, 165-171
    • Highly stereoselective hydrogenation of a pyrrole modified with chiral auxiliary had been reported; see: Hada, V.; Tungler, A.; Szepesy, L. Appl. Catal. A 2001, 210, 165-171.
  • 22
    • 38349134272 scopus 로고    scopus 로고
    • Kuwano, R.; Sawamura, M. In Catalysts for Fine Chemical Synthesis, 5: Regio- and Stereo-Controlled Oxidations and Reductions; Roberts, S. M.; Whittall, J., Eds.; John Wiley & Sons: West Sussex, 2007; pp 73-86.
    • (b) Kuwano, R.; Sawamura, M. In Catalysts for Fine Chemical Synthesis, Volume 5: Regio- and Stereo-Controlled Oxidations and Reductions; Roberts, S. M.; Whittall, J., Eds.; John Wiley & Sons: West Sussex, 2007; pp 73-86.
  • 25
    • 38349086716 scopus 로고    scopus 로고
    • See Supporting Information for details
    • See Supporting Information for details.
  • 26
    • 38349136532 scopus 로고    scopus 로고
    • 1H NMR). No enamide 3a was detected. The observation suggests that the conversion of enamide 3a into 2a will be much faster than the first hydrogenation of 1a because 3a lacks aromaticity.
    • 1H NMR). No enamide 3a was detected. The observation suggests that the conversion of enamide 3a into 2a will be much faster than the first hydrogenation of 1a because 3a lacks aromaticity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.