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Volumn 11, Issue 12, 2009, Pages 2543-2545

Catalyst-free alkylation of sulfinic acids with sulfonamides via sp 3 C-N bond cleavage at room temperature

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EID: 67149097945     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol900788r     Document Type: Article
Times cited : (106)

References (31)
  • 5
    • 67149136896 scopus 로고    scopus 로고
    • For reviews, see: (a) Simpkins, N. S. Sulfones in Organic Synthesis: Pergamon Press: New York. 1993
    • For reviews, see: (a) Simpkins, N. S. Sulfones in Organic Synthesis: Pergamon Press: New York. 1993
  • 17
    • 0344887064 scopus 로고    scopus 로고
    • 2H is 7.1. See: Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456-463.
    • 2H is 7.1. See: Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456-463.
  • 18
    • 0001097869 scopus 로고
    • For a review, see: a, Trost, B. M, Fleming, I, Eds, Pergamon Press: Oxford
    • For a review, see: (a) Solladie, G. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991, Vol. 6, pp 133-170.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 133-170
    • Solladie, G.1
  • 19
    • 17444415379 scopus 로고    scopus 로고
    • For examples, see: b
    • For examples, see: (b) Wu, J.-P.; Emeigh, J.; Su, X.-P. Org. Lett. 2005, 7, 1223-1225
    • (2005) Org. Lett , vol.7 , pp. 1223-1225
    • Wu, J.-P.1    Emeigh, J.2    Su, X.-P.3
  • 21
    • 67149142191 scopus 로고    scopus 로고
    • 1H NMR analysis of the reaction mixture.
    • 1H NMR analysis of the reaction mixture.
  • 22
    • 67149138495 scopus 로고    scopus 로고
    • 1H NMR analysis of the reaction mixture.
    • 1H NMR analysis of the reaction mixture.
  • 23
    • 67149140014 scopus 로고    scopus 로고
    • For examples on the ambident nucleophilicity of sulfinate anions toward carbon electrophiles, see: (a) Reference 10b
    • For examples on the ambident nucleophilicity of sulfinate anions toward carbon electrophiles, see: (a) Reference 10b
  • 26
    • 34347262098 scopus 로고    scopus 로고
    • For reviews on the preparation and application of such highly functionalized sulfonamides, see: a
    • For reviews on the preparation and application of such highly functionalized sulfonamides, see: (a) Masson, G.; Housseman, C.; Zhu, J. Angew. Chem., Int. Ed. 2007, 46, 4614-4628
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 4614-4628
    • Masson, G.1    Housseman, C.2    Zhu, J.3
  • 28
    • 0038778548 scopus 로고    scopus 로고
    • For the stereoselective synthesis of trisubstituted allyl sulfones, see: a
    • For the stereoselective synthesis of trisubstituted allyl sulfones, see: (a) Kabalka, G. W.; Venkataiah, B.; Dong, G. Tetrahedron Lett. 2003, 44, 4673-4675
    • (2003) Tetrahedron Lett , vol.44 , pp. 4673-4675
    • Kabalka, G.W.1    Venkataiah, B.2    Dong, G.3
  • 31
    • 67149089094 scopus 로고    scopus 로고
    • The stereochemistry of new products 2v, 2w, and 2y was assigned by 2D NOESY analysis, and the stereochemistry of new product 2s was assigned by analogy. For details, see the Supporting Information.
    • The stereochemistry of new products 2v, 2w, and 2y was assigned by 2D NOESY analysis, and the stereochemistry of new product 2s was assigned by analogy. For details, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.