메뉴 건너뛰기




Volumn 50, Issue 46, 2009, Pages 6286-6289

An efficient synthesis of Baylis-Hillman adducts of acrylamide: Pd-catalyzed hydration of Baylis-Hillman adducts of acrylonitrile

Author keywords

Acetaldoxime; Amide; Baylis Hillman adducts; Hydration; Nitrile; Palladium

Indexed keywords

ACETALDOXIME; ACRYLAMIDE; ACRYLONITRILE; NITRILE; PALLADIUM;

EID: 70349509820     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.08.127     Document Type: Article
Times cited : (28)

References (58)
  • 1
    • 0037366617 scopus 로고    scopus 로고
    • For the general review on Baylis-Hillman reaction, see:
    • For the general review on Baylis-Hillman reaction, see:. Basavaiah D., Rao A.J., and Satyanarayana T. Chem. Rev. 103 (2003) 811-891
    • (2003) Chem. Rev. , vol.103 , pp. 811-891
    • Basavaiah, D.1    Rao, A.J.2    Satyanarayana, T.3
  • 3
    • 0000892247 scopus 로고    scopus 로고
    • Paquette L.A. (Ed), John Wiley & Sons, New York
    • Ciganek E. In: Paquette L.A. (Ed). Organic Reactions Vol. 51 (1997), John Wiley & Sons, New York 201-350
    • (1997) Organic Reactions , vol.51 , pp. 201-350
    • Ciganek, E.1
  • 12
    • 4644231912 scopus 로고    scopus 로고
    • For the synthesis of Baylis-Hillman adducts of acrylamides, see:
    • For the synthesis of Baylis-Hillman adducts of acrylamides, see:. Faltin C., Fleming E.M., and Connon S.J. J. Org. Chem. 69 (2004) 6496-6499
    • (2004) J. Org. Chem. , vol.69 , pp. 6496-6499
    • Faltin, C.1    Fleming, E.M.2    Connon, S.J.3
  • 24
    • 0013298724 scopus 로고    scopus 로고
    • For the biotransformation of nitriles to amides, see:
    • For the biotransformation of nitriles to amides, see:. Wang M.-X., and Wu Y. Org. Biomol. Chem. 1 (2003) 535-540
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 535-540
    • Wang, M.-X.1    Wu, Y.2
  • 26
    • 33746580710 scopus 로고    scopus 로고
    • For the synthesis and synthetic applications of amide-containing Baylis-Hillman adducts, see:
    • For the synthesis and synthetic applications of amide-containing Baylis-Hillman adducts, see:. Singh V., Yadav G.P., Maulik P.R., and Batra S. Tetrahedron 62 (2006) 8731-8739
    • (2006) Tetrahedron , vol.62 , pp. 8731-8739
    • Singh, V.1    Yadav, G.P.2    Maulik, P.R.3    Batra, S.4
  • 35
    • 0036589307 scopus 로고    scopus 로고
    • and further references cited therein
    • Kukushkin V.Y., and Pombeiro A.J.L. Chem. Rev. 102 (2002) 1771-1802 and further references cited therein
    • (2002) Chem. Rev. , vol.102 , pp. 1771-1802
    • Kukushkin, V.Y.1    Pombeiro, A.J.L.2
  • 36
    • 14544273218 scopus 로고    scopus 로고
    • For the hydration of nitriles to amides catalyzed by acid or base, see: and further references cited therein
    • For the hydration of nitriles to amides catalyzed by acid or base, see:. Moorthy J.N., and Singhal N. J. Org. Chem. 70 (2005) 1926-1929 and further references cited therein
    • (2005) J. Org. Chem. , vol.70 , pp. 1926-1929
    • Moorthy, J.N.1    Singhal, N.2
  • 44
    • 44049100990 scopus 로고    scopus 로고
    • For the transition metal-catalyzed hydration of nitriles to amides, see:
    • For the transition metal-catalyzed hydration of nitriles to amides, see:. Goto A., Endo K., and Saito S. Angew. Chem., Int. Ed. 47 (2008) 3607-3609
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 3607-3609
    • Goto, A.1    Endo, K.2    Saito, S.3
  • 57
    • 70349517819 scopus 로고    scopus 로고
    • note
    • 3: C, 65.74; H, 5.98; N, 6.39. Found: C, 65.79; H, 6.07; N, 6.15.
  • 58
    • 70349539596 scopus 로고    scopus 로고
    • note
    • 2b described that they failed to prepare compound 2i.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.