메뉴 건너뛰기




Volumn 54, Issue 40, 2015, Pages 11780-11784

N-Heterocyclic Carbene Catalyzed Synthesis of δ-Sultones via α,β-Unsaturated Sulfonyl Azolium Intermediates

Author keywords

N heterocyclic carbenes; nucleophilic catalysis; organocatalysis; sulfonyl azolium intermediates; sulfonyl fluorides

Indexed keywords

CATALYSIS; RATE CONSTANTS; SYNTHESIS (CHEMICAL);

EID: 84942363567     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201504633     Document Type: Article
Times cited : (65)

References (50)
  • 3
    • 84861558506 scopus 로고    scopus 로고
    • (cascade catalysis)
    • Angew. Chem. 2012, 124, 320 (cascade catalysis);
    • (2012) Angew. Chem. , vol.124 , pp. 320
  • 6
    • 84922828046 scopus 로고    scopus 로고
    • (applications in total synthesis)
    • Angew. Chem. 2012, 124, 11854 (applications in total synthesis);
    • (2012) Angew. Chem. , vol.124 , pp. 11854
  • 10
    • 84922799529 scopus 로고    scopus 로고
    • (reactions with esters)
    • Angew. Chem. 2014, 126, 1509 (reactions with esters);
    • (2014) Angew. Chem. , vol.126 , pp. 1509
  • 15
    • 81955163248 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 8562.
    • (2011) Angew. Chem. , vol.123 , pp. 8562
  • 19
    • 79955661586 scopus 로고    scopus 로고
    • Angew. Chem. 2004, 116, 6331;
    • (2004) Angew. Chem. , vol.116 , pp. 6331
  • 21
    • 84894254223 scopus 로고    scopus 로고
    • For a review on NHC-catalyzed reactions with acyl azolium and azolium enolate intermediates, see:, J. Mahatthananchai, J. W. Bode, Acc. Chem. Res. 2014, 47, 696.
    • (2014) Acc. Chem. Res. , vol.47 , pp. 696
    • Mahatthananchai, J.1    Bode, J.W.2
  • 22
    • 84867447245 scopus 로고    scopus 로고
    • For a review on the synthesis and applications of sultones, see:, S. Mondal, Chem. Rev. 2012, 112, 5339.
    • (2012) Chem. Rev. , vol.112 , pp. 5339
    • Mondal, S.1
  • 27
    • 33947457223 scopus 로고
    • 2-Phenyl-ESF was reported in 1954 as a useful dienophile, but has received no attention since; see:, W. E. Truce, F. D. Hoerger, J. Am. Chem. Soc. 1954, 76, 3230.
    • (1954) J. Am. Chem. Soc. , vol.76 , pp. 3230
    • Truce, W.E.1    Hoerger, F.D.2
  • 30
    • 84942371516 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 9584; for applications in polymerization catalysis, see:
    • (2014) Angew. Chem. , vol.126 , pp. 9584
  • 32
    • 84942369028 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 9620.
    • (2014) Angew. Chem. , vol.126 , pp. 9620
  • 39
    • 84900856669 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 9319.
    • (2013) Angew. Chem. , vol.125 , pp. 9319
  • 40
    • 46449094850 scopus 로고    scopus 로고
    • V. Gembus, F. Marsais, V. Levacher, Synlett 2008, 1463; for a review comparing the reactivity of different nucleophilic catalysts in common reactions, see:
    • (2008) Synlett , pp. 1463
    • Gembus, V.1    Marsais, F.2    Levacher, V.3
  • 43
    • 84942367699 scopus 로고    scopus 로고
    • Angew. Chem. 2010, 122, 2726;
    • (2010) Angew. Chem. , vol.122 , pp. 2726
  • 44
    • 77952821762 scopus 로고    scopus 로고
    • for an NHC-catalyzed sulfone rearrangement, see
    • A.-N. R. Alba, X. Companyõ, R. Rios, Chem. Soc. Rev. 2010, 39, 2018; for an NHC-catalyzed sulfone rearrangement, see:
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 2018
    • Alba, A.-N.R.1    Companyõ, X.2    Rios, R.3
  • 50
    • 84865842424 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 5325.
    • (2012) Angew. Chem. , vol.124 , pp. 5325


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.