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Volumn 11, Issue 6, 2009, Pages 1369-1372

A direct phosphine-mediated synthesis of pyrroles from acid chlorides and α,β-unsaturated imines

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; IMINE; LUKIANOL A; PHOSPHINE; PHOSPHINE DERIVATIVE; PYRAZOLE DERIVATIVE; PYRROLE DERIVATIVE;

EID: 64049086638     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol900185n     Document Type: Article
Times cited : (78)

References (71)
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    • For general biological activity of pyrroles, see
    • (c) Bailly, C. Curr. Med. Chem. Anti-Cancer Agents 2004, 4, 363-378. For general biological activity of pyrroles, see:
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    • Paal, C.1
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    • For reviews, see: a, Katritzky, A. R, Rees, C. W, Scriven, E. F. V, Eds, Pergamon: Oxford
    • For reviews, see: (a) Sundberg, R. J. In ComprehensiVe Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.; Pergamon: Oxford, 1996; Vol. 2.
    • (1996) ComprehensiVe Heterocyclic Chemistry , vol.2
    • Sundberg, R.J.1
  • 24
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    • Maas, G, Ed, Thieme: New York
    • (b) Black, D. S. C. In Science of Synthesis; Maas, G, Ed.; Thieme: New York, 2001; Vol. 9.
    • (2001) Science of Synthesis , vol.9
    • Black, D.S.C.1
  • 32
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    • Recent examples: (a) Mihovilovic, M. D.; Stanetty, P. Angew. Chem., Int. Ed. 2007, 46, 3612-3615.
    • Recent examples: (a) Mihovilovic, M. D.; Stanetty, P. Angew. Chem., Int. Ed. 2007, 46, 3612-3615.
  • 48
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    • For the synthesis of pyrroles via aza-Wittig reagents and other phosphine-mediated pyrrole syntheses, see: (a) Eguchi, S. ARKIVOC 2005, 2, 98-119
    • For the synthesis of pyrroles via aza-Wittig reagents and other phosphine-mediated pyrrole syntheses, see: (a) Eguchi, S. ARKIVOC 2005, 2, 98-119.
  • 61
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    • Complex 4 cannot be isolated from the reaction mixture; however, its spectroscopic data
    • Complex 4 cannot be isolated from the reaction mixture; however, its spectroscopic data
  • 62
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    • 12
    • 12
  • 71
    • 64349113481 scopus 로고    scopus 로고
    • Steps c-f follow the protocol developed by Fürstner in ref 19a.
    • Steps c-f follow the protocol developed by Fürstner in ref 19a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.