메뉴 건너뛰기




Volumn 71, Issue 1, 2006, Pages 210-214

Oxidation of aromatic lithium thiolates into sulfinate salts: An attractive entry to aryl sulfones labeled with carbon-11

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBONS; CARBON; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PURIFICATION;

EID: 31144467338     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo051942v     Document Type: Article
Times cited : (36)

References (67)
  • 2
    • 0036389509 scopus 로고    scopus 로고
    • (b) Elsinga, P. H. Methods 2002, 27, 208-217.
    • (2002) Methods , vol.27 , pp. 208-217
    • Elsinga, P.H.1
  • 4
    • 84953397956 scopus 로고
    • Biological activity of sulfoxides and sulfones
    • Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, Chapter 16
    • (a) Kalir, R.; Kalir, H. H. Biological Activity of Sulfoxides and Sulfones. In The Chemistry of Sulphur-containing Functional Group; Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, 1993; Chapter 16, pp 957-973.
    • (1993) The Chemistry of Sulphur-containing Functional Group , pp. 957-973
    • Kalir, R.1    Kalir, H.H.2
  • 23
    • 0013496806 scopus 로고    scopus 로고
    • See also references cited in the following: (t) Baskin, J. M.; Wang, Z. Org. Lett. 2002, 4, 4423-4425.
    • (2002) Org. Lett. , vol.4 , pp. 4423-4425
    • Baskin, J.M.1    Wang, Z.2
  • 33
  • 39
    • 0012049015 scopus 로고    scopus 로고
    • For Information about syntheses of sulfones, see the following: (a) Ward, R. S.; Diaper, R. L. Sulfur Rep. 2001, 22, 251-275.
    • (2001) Sulfur Rep. , vol.22 , pp. 251-275
    • Ward, R.S.1    Diaper, R.L.2
  • 40
    • 0003869660 scopus 로고
    • Baldwin, J. E., Magnus, P. D., Eds.; Pergamon Press: Oxford
    • (b) Simpkins, N. S. In Sulphones in Organic Synthesis; Baldwin, J. E., Magnus, P. D., Eds.; Pergamon Press: Oxford, 1993; Vol. 10.
    • (1993) Sulphones in Organic Synthesis , vol.10
    • Simpkins, N.S.1
  • 55
    • 17444415379 scopus 로고    scopus 로고
    • Sulfinates are ambident nucleophiles. With soft electrophiles such as alkyl halides the alkylation occurs predominantly at sulfur to give sulfones: (a) 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
  • 67
    • 31144454561 scopus 로고    scopus 로고
    • note
    • The weight of the sulfinate salt was slightly superior because of remaining water.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.