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Volumn 74, Issue 10, 2009, Pages 3993-3996

Catalytic asymmetric syntheses of α-amino and α-hydroxyl acid derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ACID DERIVATIVE; ARYL BROMIDES; ASYMMETRIC HYDROGENATION; ASYMMETRIC SYNTHESIS; CHEMICAL EQUATIONS; CHEMICAL YIELDS; HECK REACTIONS; ROOM TEMPERATURE;

EID: 65949124020     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900368k     Document Type: Article
Times cited : (16)

References (29)
  • 19
    • 65949103157 scopus 로고    scopus 로고
    • Reference 6.
    • (c) Reference 6.
  • 23
    • 0027397575 scopus 로고
    • (c) For the mechanistic study of the asymmetric hydrogenation of enamides employing Burk's catalyst, see:
    • (c) For the mechanistic study of the asymmetric hydrogenation of enamides employing Burk's catalyst, see: Armstrong, S. K.; Brown, J. M.; Burk, M. J. Tetrahedron Lett. 1993, 34, 879-882.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 879-882
    • Armstrong, S.K.1    Brown, J.M.2    Burk, M.J.3
  • 24
    • 55249085822 scopus 로고    scopus 로고
    • (d) For our recent asymmetric syntheses of tyrosine surrogates using Burk's rhodium complex of EtDuphos, see:
    • (d) For our recent asymmetric syntheses of tyrosine surrogates using Burk's rhodium complex of EtDuphos, see: Han, X.; Civiello, R. L.; Fang, H.; Wu, D.; Gao, Q.; Chaturvedula, P. V.; Macor, J. E.; Dubowchik, G. M. J. Org. Chem. 2008, 73, 8502-8510.
    • (2008) J. Org. Chem. , vol.73 , pp. 8502-8510
    • Han, X.1    Civiello, R.L.2    Fang, H.3    Wu, D.4    Gao, Q.5    Chaturvedula, P.V.6    Macor, J.E.7    Dubowchik, G.M.8
  • 27
    • 65949083081 scopus 로고
    • 4Cl was first reported by Shih to reduce aromatic nitro compounds, see:
    • 4Cl was first reported by Shih to reduce aromatic nitro compounds, see: Shih, Y.-T. Huaxue Xuebao 1956, 22, 352-355.
    • (1956) Huaxue Xuebao , vol.22 , pp. 352-355
    • Shih, Y.-T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.