메뉴 건너뛰기




Volumn 75, Issue 18, 2010, Pages 6271-6274

Synthesis of highly substituted pyrroles via nucleophilic catalysis

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATED ALKYNES; CONCISE SYNTHESIS; IN-SITU; INTERMOLECULAR ADDITIONS; NUCLEOPHILIC CATALYSIS; ONE-POT METHOD; REGIO-SELECTIVE; THERMAL REARRANGEMENT;

EID: 77956537793     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1011448     Document Type: Article
Times cited : (77)

References (28)
  • 4
    • 33747139387 scopus 로고    scopus 로고
    • For example, see
    • For example, see: Bellina, F.; Rossi, R. Tetrahedron 2006, 62, 7213-7256
    • (2006) Tetrahedron , vol.62 , pp. 7213-7256
    • Bellina, F.1    Rossi, R.2
  • 10
    • 1342285524 scopus 로고    scopus 로고
    • For a recent microwave-assisted Paal-Knorr pyrrole synthesis, see
    • For a recent microwave-assisted Paal-Knorr pyrrole synthesis, see: Minetto, G.; Raveglia, L. F.; Taddei, M. Org. Lett. 2004, 6, 389-392
    • (2004) Org. Lett. , vol.6 , pp. 389-392
    • Minetto, G.1    Raveglia, L.F.2    Taddei, M.3
  • 11
    • 0033546105 scopus 로고    scopus 로고
    • For examples of the use of the Trofimov reaction in synthesis, see
    • For examples of the use of the Trofimov reaction in synthesis, see: Gonzales, F.; Sanz-Cervera, J. F.; William, R. M. Tetrahedron Lett. 1999, 40, 4519-4522
    • (1999) Tetrahedron Lett. , vol.40 , pp. 4519-4522
    • Gonzales, F.1    Sanz-Cervera, J.F.2    William, R.M.3
  • 17
    • 0034867881 scopus 로고    scopus 로고
    • 3 as a nucleophilic catalyst, see
    • 3 as a nucleophilic catalyst, see: Lu, X.; Zhang, C.; Xu, Z. Acc. Chem. Res. 2001, 34, 535-544
    • (2001) Acc. Chem. Res. , vol.34 , pp. 535-544
    • Lu, X.1    Zhang, C.2    Xu, Z.3
  • 18
    • 38449098180 scopus 로고    scopus 로고
    • For a related nucleophilic catalysis approach to N -hydroxy pyrroles, see:;;, - 103 and references therein
    • For a related nucleophilic catalysis approach to N -hydroxy pyrroles, see: Hekmatshoar, R.; Nouri, R.; Beheshtiha, S. Y. S. Heteroat. Chem. 2008, 19, 100 - 103 and references therein.
    • (2008) Heteroat. Chem. , vol.19 , pp. 100
    • Hekmatshoar, R.1    Nouri, R.2    Beheshtiha, S.Y.S.3
  • 19
    • 8444241193 scopus 로고    scopus 로고
    • For use of nucleophilic catalysts in the related Morita-Baylis-Hillman reaction, see
    • For use of nucleophilic catalysts in the related Morita-Baylis-Hillman reaction, see: Spivey, A. C.; Areniyadis, S. Angew. Chem., Int. Ed. 2004, 43, 5436-5441
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 5436-5441
    • Spivey, A.C.1    Areniyadis, S.2
  • 21
    • 34548275917 scopus 로고    scopus 로고
    • For a review on microwave-assisted multicomponent reactions for the synthesis of heterocycles, see
    • For a review on microwave-assisted multicomponent reactions for the synthesis of heterocycles, see: Bagley, M. C.; Lubinu, M. C. Top. Heterocycl. Chem. 2006, 31-58
    • (2006) Top. Heterocycl. Chem. , pp. 31-58
    • Bagley, M.C.1    Lubinu, M.C.2
  • 27
    • 77956522818 scopus 로고    scopus 로고
    • note
    • See Supporting Information for details on the synthesis and characterization of oximes 1a - 1k.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.