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Volumn 17, Issue 26, 2011, Pages 7183-7187

Regioselective synthesis of 3-substituted pyrroles by nucleophilic addition of 3-(1-arylsulfonylalkyl) pyrroles activated under basic or acid conditions

Author keywords

carbonyl compounds; heterocycles; imino compounds; nucleophilic addition; pyrroles

Indexed keywords

ACID CONDITIONS; ACIDIC CONDITIONS; HETEROCYCLES; IMINO COMPOUNDS; NUCLEOPHILIC ADDITIONS; NUCLEOPHILIC REAGENT; PYRROLES; REGIOSELECTIVE SYNTHESIS;

EID: 79958806243     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201100434     Document Type: Article
Times cited : (20)

References (49)
  • 4
    • 71949117774 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9608-9644.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9608-9644
  • 25
    • 44949166937 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 3004-3007
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3004-3007
  • 34
    • 55249108726 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 8707-8710
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8707-8710
  • 35
    • 78349295979 scopus 로고    scopus 로고
    • for a recent perspective on the utilization of alkylideneindolenine intermediates in synthesis, see
    • R. Ballini, S. Gabrielli, A. Palmieri, M. Petrini, Adv. Synth. Catal. 2010, 352, 2459-2462; for a recent perspective on the utilization of alkylideneindolenine intermediates in synthesis, see
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 2459-2462
    • Ballini, R.1    Gabrielli, S.2    Palmieri, A.3    Petrini, M.4
  • 37
    • 79951843028 scopus 로고    scopus 로고
    • Very recently, stable alkylideneindolenine compounds have been prepared by palladium-catalyzed reaction of alkynylimines with aryl iodides:,. The 1,4-type regioselectivity and reactivity observed in nucleophilic additions to intermediate 2 a probably stems from the major contribution of the resonance structure 2 a″ involving charge separation with aromatic character
    • Very recently, stable alkylideneindolenine compounds have been prepared by palladium-catalyzed reaction of alkynylimines with aryl iodides:, Z. Chen, J. Zhu, H. Xie, S. Li, Y. Wu, Y. Gong, Adv. Synth. Catal. 2011, 353, 325-330. The 1,4-type regioselectivity and reactivity observed in nucleophilic additions to intermediate 2 a probably stems from the major contribution of the resonance structure 2 a″ involving charge separation with aromatic character.
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 325-330
    • Chen, Z.1    Zhu, J.2    Xie, H.3    Li, S.4    Wu, Y.5    Gong, Y.6
  • 40
    • 79958806032 scopus 로고    scopus 로고
    • Unclean reaction mixtures were indeed obtained by using N-benzyl, N-Boc, and N-TBDMS pyrrole derivatives
    • Unclean reaction mixtures were indeed obtained by using N-benzyl, N-Boc, and N-TBDMS pyrrole derivatives.
  • 41
    • 79958825264 scopus 로고    scopus 로고
    • It has been demonstrated that no free fluoride anions are present in potassium fluoride on basic alumina
    • It has been demonstrated that no free fluoride anions are present in potassium fluoride on basic alumina
  • 46
    • 0038372733 scopus 로고    scopus 로고
    • For a recent double addition involving malononitrile in a domino process, see
    • Y. I. Binev, J. A. Tsenov, I. N. Juchnovski, I. G. Binev, J. Mol. Struct. 2003, 625, 207-214. For a recent double addition involving malononitrile in a domino process, see
    • (2003) J. Mol. Struct. , vol.625 , pp. 207-214
    • Binev, Y.I.1    Tsenov, J.A.2    Juchnovski, I.N.3    Binev, I.G.4
  • 48
    • 34248192461 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1101-1104.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1101-1104
  • 49
    • 79958862548 scopus 로고    scopus 로고
    • 2 leading to pyrrole 12 (see the Supporting Information for details)
    • 2 leading to pyrrole 12 (see the Supporting Information for details).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.