메뉴 건너뛰기




Volumn 17, Issue 35, 1976, Pages 3001-3004

Organic sulfur chemistry. XXI. Trisulfide formation by alkoxide decomposition of sulfenylthiocarbonates

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000768015     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(76)80054-8     Document Type: Article
Times cited : (30)

References (15)
  • 1
    • 84914231441 scopus 로고    scopus 로고
    • D.N. Harpp and A. Granata unpublished results.
  • 5
    • 84914231440 scopus 로고    scopus 로고
    • At present no widely useful procedure is available for the synthesis of this class of compounds.
  • 6
    • 84914231439 scopus 로고    scopus 로고
    • There is no reaction between 1 and alcohols.
  • 7
    • 84971037712 scopus 로고
    • Monothiocarbonates and their oxidation to disulphides
    • It was further noted that salt 5 showed an ultra violet absorption at 221 nm in excellent agreement with that published for 5 (222 nm);
    • (1973) Australian Journal of Chemistry , vol.26 , pp. 755
    • Murphy1    Winter2
  • 10
    • 0016382398 scopus 로고
    • 3 180.0093; found: 180.0103; Rast molecular weight determination (camphor) 196, 213. Attempts to purify 7 without column chromatography resulted in a much lower yield of monomer. To our knowledge, compound 7 is the largest monocyclic trisulfide reported to date: cf., for an unsaturated bicyclic case.
    • (1974) Tetrahedron Lett. , pp. 1659
    • Fritz1    Weis2
  • 15
    • 84914231438 scopus 로고    scopus 로고
    • After column chromatography, 6 gave a homogeneous tlc as well as a pmr spectrum consistent with its structure.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.