Preparation of Medium-Ring Lactones and Lactams by Electrophilic Cyclizations

This publication has 8 references indexed in Scilit:

• Preparation of Oxepanes, Oxepenes, and Oxocanes by Iodoetherification using Bis(sym-collidine)iodine(I) Hexafluorophosphate as Electrophile
  The Journal of Organic Chemistry, 1996
• Oxygen Effect in the Iodo Lactonization of Unsaturated Carboxylic Acids Leading to 7- to 12-Membered Ring Lactones
  The Journal of Organic Chemistry, 1994
• Gem-dimethyl effect in the formation of seven to eleven-membered ring lactones by iodolactonisation
  Tetrahedron Letters, 1993
• Carboxylation of carbenes in low-temperature matrixes
  The Journal of Organic Chemistry, 1992
• Iterative synthesis of selectively substituted .alpha.,.beta.-unsaturated and saturated medium-ring lactones
  The Journal of Organic Chemistry, 1990
• Ring closure reactions of bifunctional chain molecules
  Accounts of Chemical Research, 1981
• Nucleophilic borohydride: selective reductive displacement of halides, sulfonate esters, tertiary amines, and N,N-disulfonimides with borohydride reagents in polar aprotic solvents
  The Journal of Organic Chemistry, 1978
• Reduction of epoxides to olefins with low valent titanium
  The Journal of Organic Chemistry, 1975