메뉴 건너뛰기




Volumn 40, Issue 24, 1999, Pages 4555-4558

A general synthesis of 2-formyl-3-arylpyrroles

Author keywords

Arylboronic acids; Biaryls; Coupling reactions; Palladium catalyst; Pyrrole derivatives

Indexed keywords

CINNAMALDEHYDE; PALLADIUM; PYRROLE DERIVATIVE;

EID: 0033546374     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00808-4     Document Type: Article
Times cited : (48)

References (28)
  • 2
    • 85007898294 scopus 로고
    • 2. Tanaka, K.; Kariyone, E.; Umio, S. Chem. Pharm. Bull. 1969, 17, 611-615. Ratcliffe, A.H.; Smith, G.F.; Smith, G.N. Tetrahedron Lett. 1973, 52, 5179-5184. Albini, A.; Fasani, E. and Lohse, C. Heterocycles 1988, 27, 113-124 and references cited herein. Alberola, A. J. Chem. Soc. Perkin Trans. 1 1990, 2681-2685. Arnold, D.P.; Burgess-Dean, L.; Hibbard, J. and Abdur Rahman M. Aust. J. Chem. 1994, 47, 969-974.
    • (1969) Chem. Pharm. Bull. , vol.17 , pp. 611-615
    • Tanaka, K.1    Kariyone, E.2    Umio, S.3
  • 3
    • 0001436902 scopus 로고
    • Tanaka, K.; Kariyone, E.; Umio, S. Chem. Pharm. Bull. 1969, 17, 611-615. Ratcliffe, A.H.; Smith, G.F.; Smith, G.N. Tetrahedron Lett. 1973, 52, 5179-5184. Albini, A.; Fasani, E. and Lohse, C. Heterocycles 1988, 27, 113-124 and references cited herein. Alberola, A. J. Chem. Soc. Perkin Trans. 1 1990, 2681-2685. Arnold, D.P.; Burgess-Dean, L.; Hibbard, J. and Abdur Rahman M. Aust. J. Chem. 1994, 47, 969-974.
    • (1973) Tetrahedron Lett. , vol.52 , pp. 5179-5184
    • Ratcliffe, A.H.1    Smith, G.F.2    Smith, G.N.3
  • 4
    • 0013594606 scopus 로고
    • and references cited herein
    • Tanaka, K.; Kariyone, E.; Umio, S. Chem. Pharm. Bull. 1969, 17, 611-615. Ratcliffe, A.H.; Smith, G.F.; Smith, G.N. Tetrahedron Lett. 1973, 52, 5179-5184. Albini, A.; Fasani, E. and Lohse, C. Heterocycles 1988, 27, 113-124 and references cited herein. Alberola, A. J. Chem. Soc. Perkin Trans. 1 1990, 2681-2685. Arnold, D.P.; Burgess-Dean, L.; Hibbard, J. and Abdur Rahman M. Aust. J. Chem. 1994, 47, 969-974.
    • (1988) Heterocycles , vol.27 , pp. 113-124
    • Albini, A.1    Fasani, E.2    Lohse, C.3
  • 5
    • 37049082297 scopus 로고
    • Tanaka, K.; Kariyone, E.; Umio, S. Chem. Pharm. Bull. 1969, 17, 611-615. Ratcliffe, A.H.; Smith, G.F.; Smith, G.N. Tetrahedron Lett. 1973, 52, 5179-5184. Albini, A.; Fasani, E. and Lohse, C. Heterocycles 1988, 27, 113-124 and references cited herein. Alberola, A. J. Chem. Soc. Perkin Trans. 1 1990, 2681-2685. Arnold, D.P.; Burgess-Dean, L.; Hibbard, J. and Abdur Rahman M. Aust. J. Chem. 1994, 47, 969-974.
    • (1990) J. Chem. Soc. Perkin Trans. 1 , pp. 2681-2685
    • Alberola, A.1
  • 6
    • 0000591764 scopus 로고
    • Tanaka, K.; Kariyone, E.; Umio, S. Chem. Pharm. Bull. 1969, 17, 611-615. Ratcliffe, A.H.; Smith, G.F.; Smith, G.N. Tetrahedron Lett. 1973, 52, 5179-5184. Albini, A.; Fasani, E. and Lohse, C. Heterocycles 1988, 27, 113-124 and references cited herein. Alberola, A. J. Chem. Soc. Perkin Trans. 1 1990, 2681-2685. Arnold, D.P.; Burgess-Dean, L.; Hibbard, J. and Abdur Rahman M. Aust. J. Chem. 1994, 47, 969-974.
    • (1994) Aust. J. Chem. , vol.47 , pp. 969-974
    • Arnold, D.P.1    Burgess-Dean, L.2    Hibbard, J.3    Abdur Rahman, M.4
  • 15
    • 0032518829 scopus 로고    scopus 로고
    • 4. a) Recent review : Stanforth, S.P. Tetrahedron 1998, 54, 263-303. See also
    • (1998) Tetrahedron , vol.54 , pp. 263-303
    • Stanforth, S.P.1
  • 25
    • 33751385493 scopus 로고
    • 9. Oh-e, T.; Miyaura, N. and Suzuki, A. J. Org. Chem. 1993, 58, 2201-2208. For a recent example, see :Mohri, S.; Stefinovic, M. and Snieckus, V. J. Org. Chem. 1997, 62, 7072-7073.
    • (1993) J. Org. Chem. , vol.58 , pp. 2201-2208
    • Oh-e, T.1    Miyaura, N.2    Suzuki, A.3
  • 26
    • 0030819305 scopus 로고    scopus 로고
    • 9. Oh-e, T.; Miyaura, N. and Suzuki, A. J. Org. Chem. 1993, 58, 2201-2208. For a recent example, see : Mohri, S.; Stefinovic, M. and Snieckus, V. J. Org. Chem. 1997, 62, 7072-7073.
    • (1997) J. Org. Chem. , vol.62 , pp. 7072-7073
    • Mohri, S.1    Stefinovic, M.2    Snieckus, V.3
  • 27
    • 0013593758 scopus 로고    scopus 로고
    • note
    • +. Anal. calcd. : C 58.37%; H 3.81%; N 7.56%. Found : C 58.23%; H 3.56%; N 7.37%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.