Convenient method for the addition of disulfides to alkenes

Bioorganic and Medicinal Chemistry Letters

Volumn 17, Issue 22, 2007, Pages 6197-6201

  Yamagiwa, Noriyuki ^a   Suto, Yutaka ^a   Torisawa, Yasuhiro ^a  

^a TAKASAKI UNIVERSITY OF HEALTH AND WELFARE   (Japan)

Author keywords

Alkene; Alkyne; Disulfide; Lewis acid; Sulfenylation

Indexed keywords

ALKENE DERIVATIVE; ALUMINUM CHLORIDE; CYCLOALKENE; DISULFIDE; FERRIC CHLORIDE; LEWIS ACID;

ADDITION REACTION; ARTICLE; BIOTRANSFORMATION; CATALYSIS; CATALYST; CHEMICAL REACTION; DISULFENYLATION; FEASIBILITY STUDY; POLYMERIZATION; QUANTUM YIELD; REACTION ANALYSIS; STEREOCHEMISTRY;

ALKENES; CATALYSIS; CYCLOPARAFFINS; DISULFIDES; FERRIC COMPOUNDS; MOLECULAR STRUCTURE;

EID: 35148828561     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.09.021     Document Type: Article

References (11)

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7. +]: 350.1157; found: 350.1152.
8. Reaction mechanism of these disulfenylation reactions was well discussed in Refs. 2 and 4.
9. Disulfenylation of 1,3-cyclohexadiene afforded a complex mixture of 1,2- and 1,4-adducts.
10. +.
11. 3 catalyst, (E)-8 easily isomerized to (Z)-8. The mechanism of isomerization is under investigation.{A figure is presented}.