메뉴 건너뛰기




Volumn 13, Issue 4, 2007, Pages 1032-1046

A fluorous, pummerer cyclative-capture strategy for the synthesis of N-heterocycles

Author keywords

Fluorous phase synthesis; Heterocycles; Organic synthesis; Pummerer reaction; Samarium

Indexed keywords

AROMATIZATION; CHEMICAL MODIFICATION; FLUORINE; OXIDATION; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 33846615046     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200601429     Document Type: Article
Times cited : (50)

References (62)
  • 2
    • 33846621863 scopus 로고    scopus 로고
    • P. J. Crowley in Comprehensive Heterocyclic Chemistry (Eds. : A. R. Katritzky, C. W. Rees), Pergamon, New York, 1984.
    • b) P. J. Crowley in Comprehensive Heterocyclic Chemistry (Eds. : A. R. Katritzky, C. W. Rees), Pergamon, New York, 1984.
  • 4
    • 2942545969 scopus 로고    scopus 로고
    • for a review of fluorous-phase approaches in heterocycle synthesis see
    • b) for a review of fluorous-phase approaches in heterocycle synthesis see: W. Zhang, Chem. Rev. 2004, 104, 2531.
    • (2004) Chem. Rev , vol.104 , pp. 2531
    • Zhang, W.1
  • 6
    • 0348072278 scopus 로고    scopus 로고
    • For recent reviews see, a, Eds, J. A. Gladysz, D. P. Curran, I. T. Horváth, Wiley-VCH, Weinheim
    • For recent reviews see : a) D. P. Curran in The Handbook of Fluorous Chemistry (Eds.: J. A. Gladysz, D. P. Curran, I. T. Horváth), Wiley-VCH, Weinheim, 2004;
    • (2004) The Handbook of Fluorous Chemistry
    • Curran, D.P.1
  • 9
  • 11
    • 33745645688 scopus 로고    scopus 로고
    • For recent reviews on the Pummerer reaction see: a
    • For recent reviews on the Pummerer reaction see: a) K. S. Feldman, Tetrahedron 2006, 62, 5003;
    • (2006) Tetrahedron , vol.62 , pp. 5003
    • Feldman, K.S.1
  • 20
    • 0037013910 scopus 로고    scopus 로고
    • Fluorous thiols as nucleophilic scavenging reagents see: a
    • Fluorous thiols as nucleophilic scavenging reagents see: a) C. W. Lindsley, Z. Zhao, W. H. Leister, Tetrahedron Lett. 2002, 43, 4225;
    • (2002) Tetrahedron Lett , vol.43 , pp. 4225
    • Lindsley, C.W.1    Zhao, Z.2    Leister, W.H.3
  • 22
    • 0038260112 scopus 로고    scopus 로고
    • Fluorous thiols to introduce tags for multistep synthesis see: c
    • Fluorous thiols to introduce tags for multistep synthesis see: c) W. Zhang, Org. Lett. 2003, 5, 1011;
    • (2003) Org. Lett , vol.5 , pp. 1011
    • Zhang, W.1
  • 26
    • 0035819981 scopus 로고    scopus 로고
    • Similar reductions using other electron-transfer reagents have been reported: a J. M. Manthorpe, J. L. Gleason, J. Am. Chem. Soc. 2001, 123, 2091;
    • Similar reductions using other electron-transfer reagents have been reported: a) J. M. Manthorpe, J. L. Gleason, J. Am. Chem. Soc. 2001, 123, 2091;
  • 28
  • 37
    • 0035935103 scopus 로고    scopus 로고
    • The oxidation of sulfide linkers to the corresponding sulfoxide, followed by Pummerer rearrangement has been used in cleavage strategies to release alcohols and aldehydes from solid supports: a C. Rolland, G. Hanquet, J. B. Ducep, G. Solladié, Tetrahedron Lett. 2001, 42, 7563;
    • The oxidation of sulfide linkers to the corresponding sulfoxide, followed by Pummerer rearrangement has been used in cleavage strategies to release alcohols and aldehydes from solid supports: a) C. Rolland, G. Hanquet, J. B. Ducep, G. Solladié, Tetrahedron Lett. 2001, 42, 7563;
  • 44
    • 12344280348 scopus 로고    scopus 로고
    • for the first studies on rearrangements to oxindoles see
    • for the first studies on rearrangements to oxindoles see: I. D. Hills, G. C. Fu, Angew. Chem. 2003, 115, 3969;
    • (2003) Angew. Chem , vol.115 , pp. 3969
    • Hills, I.D.1    Fu, G.C.2
  • 45


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.