메뉴 건너뛰기




Volumn 48, Issue 6, 1998, Pages 1121-1138

Synthesis of 2-alkylidene-3,3-dialkyl-1,4-dithianes and their oxathiane analogues by 1,2-sulphur migration

Author keywords

[No Author keywords available]

Indexed keywords


EID: 18444398054     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-97-7898     Document Type: Article
Times cited : (6)

References (31)
  • 23
    • 0028935014 scopus 로고
    • Recently a structural rearrangement, involving C-C bond breaking and forming reactions, was induced by an α-activation process in a dithiolane, the intermediate sulphonium ion being the initiator for a process which resulted in the reformation of the dithiolane ring, K. Konno, S. Maki, S. Sagari, and H. Takayama, Tetrahedron Lett., 1995, 36, 1865.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 1865
    • Konno, K.1    Maki, S.2    Sagari, S.3    Takayama, H.4
  • 24
    • 18444396389 scopus 로고    scopus 로고
    • The stereochemistry of additions and cycloadditions to the reactive double bond should be influenced by the adjacent chiral centre
    • The stereochemistry of additions and cycloadditions to the reactive double bond should be influenced by the adjacent chiral centre.
  • 25
    • 0000977373 scopus 로고
    • We have observed that the monosulphoxidation of these dithiane systems is highly regioselective. The disulphoxidation of 1,3-dithianes, 1,3-dithiolanes and 1,4-dithiins is highly selective and always gives the trans- dioxide as the major product. V.K. Aggarwal, G. Evans, E. Moya, and J. Dowden, J. Org. Chem., 1992, 57, 6390;
    • (1992) J. Org. Chem. , vol.57 , pp. 6390
    • Aggarwal, V.K.1    Evans, G.2    Moya, E.3    Dowden, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.