메뉴 건너뛰기




Volumn 70, Issue 19, 2005, Pages 7672-7678

Is there a homolytic substitution chemistry (SH2) of sulfones?

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; DECOMPOSITION; FREE RADICALS; HYDROGEN; ORGANIC SOLVENTS; SUBSTITUTION REACTIONS;

EID: 24944534479     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050990c     Document Type: Article
Times cited : (21)

References (86)
  • 9
    • 0542360103 scopus 로고
    • Pryor, W. A., Ed.; ACS Symposium Series No. 69; American Chemical Society: Washington, DC
    • (b) Kampmeier, J. A.; Jordan, R. B.; Liu, M. S.; Yamanaka, H.; Bishop, D. J. In Organic Free Radicals; Pryor, W. A., Ed.; ACS Symposium Series No. 69; American Chemical Society: Washington, DC, 1978; p 275.
    • (1978) Organic Free Radicals , pp. 275
    • Kampmeier, J.A.1    Jordan, R.B.2    Liu, M.S.3    Yamanaka, H.4    Bishop, D.J.5
  • 36
    • 24944440731 scopus 로고    scopus 로고
    • note
    • 2a Kampmeier reports in a footnote that the sulfone corresponding to 1 (R = Me) was prepared but no comment was made on any chemistry of this sulfone.
  • 42
    • 14844302399 scopus 로고    scopus 로고
    • A recent discussion of the mechanisms of substitution of arene diazonium ions: Ussing, B. R.; Singleton, D. A. J. Am. Chem. Soc. 2005, 127, 2888.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 2888
    • Ussing, B.R.1    Singleton, D.A.2
  • 49
    • 0034649099 scopus 로고    scopus 로고
    • For related reactions involving intramolecular hydrogen abstraction by an aryl radical followed by cyclization onto the aromatic ring, see: Storey, J. M. D. Tetrahedron Lett. 2000, 41, 8173.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8173
    • Storey, J.M.D.1
  • 51
    • 0038800178 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim
    • (b) Murphy, J. A. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, p 298.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 298
    • Murphy, J.A.1
  • 57
    • 0000782249 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim
    • (c) Newcomb, M. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, p 317.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 317
    • Newcomb, M.1
  • 58
    • 0000816927 scopus 로고    scopus 로고
    • In other circumstances the aryl-substituted cyclohexadienyl radicals, such as the ones implied in the formation of either 39 or 41, may be trapped in stannane-mediated systems with catalytic diphenyl diselenide, resulting in a synthetically useful process, (a) Crich, D.; Hwang, J.-T. J. Org. Chem. 1998, 63, 2765.
    • (1998) J. Org. Chem. , vol.63 , pp. 2765
    • Crich, D.1    Hwang, J.-T.2
  • 68
    • 24944490024 scopus 로고    scopus 로고
    • note
    • 13C NMR spectrum.
  • 69
    • 24944538772 scopus 로고    scopus 로고
    • note
    • The main components of this mixture contained both an electron-rich and an electron-poor aromatic ring, suggesting that they are derived from opening of the sultine ring in 36.
  • 71
    • 24944539607 scopus 로고    scopus 로고
    • note
    • 3): -1.6, -0.2, 1.5 (9 carbons), 20.2, 21.5, 43.6, 124.8, 125.8, 129.7,131.8, 138.8, 159.6.
  • 72
    • 0002523168 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M., Eds.; Wiley-VCH: Weinheim
    • (a) Studer, A.; Bossart, M. In Radicals in Organic Synthesis; Renaud, P., Sibi, M., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 2, p 62.
    • (2001) Radicals in Organic Synthesis , vol.2 , pp. 62
    • Studer, A.1    Bossart, M.2
  • 81
    • 0009476711 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M., Eds.; Wiley-VCH: Weinheim
    • (a) Rosenstein, I. J. In Radicals in Organic synthesis; Renaud, P., Sibi, M., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, p 50.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 50
    • Rosenstein, I.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.