Ring contraction of 3-deoxy-2-O-trifluoromethanesulphonates of α-hydroxy-γ-lactones to oxetanes

This publication has 15 references indexed in Scilit:

• Ring contraction of 2-o-trifluoromethanesulphonates of α-hydroxy-γ-lactones to oxetane carboxylic esters
  Tetrahedron Letters, 1990
• Synthetic studies on new sugar oxetanose: Synthesis of D-erythrooxetanose and its reaction with silylated adenine derivative
  Tetrahedron Letters, 1990
• Evaluation of two possible transition states in intramolecular oxetane/oxolane ring formation based on AM1 calculations
  Tetrahedron Letters, 1990
• Synthesis of the potent antiviral oxetane nucleoside epinoroxetanocin from D-lyxonolactone
  Tetrahedron: Asymmetry, 1990
• Stabilisation of the thromboxane ring system by electron-withdrawing substituents. Mechanism and reactivity in the hydrolysis of alkyl and aryl oxetane acetals
  Journal of the Chemical Society, Perkin Transactions 2, 1990
• Efficacy of oxetanocin G against herpes simplex virus type 2 and murine cytomegalovirus infections in mice.
  The Journal of Antibiotics, 1989
• Chiral oxetanes from sugar lactones: Synthesis of derivatives of 3,5-anhydro-1,2-O-isopropyl-α-D-glucuronic acid and of 3,5-anhydro-1,2-O-isopropyllidene-β-L-iduronic acid
  Tetrahedron Letters, 1987
• Inhibition of infectivity of human immunodeficiency virus by oxetanocin.
  The Journal of Antibiotics, 1987
• Oxetanocin, a novel nucleoside from bacteria.
  The Journal of Antibiotics, 1986
• Branched-chain sugar nucleosides. I. 9-[3-Deoxy-3-C-(2-hydroxyethyl)-.beta.-D-allofuranosyl]adenine and 9-[3-deoxy-3-C-(2-hydroxyethyl)-.beta.-D-ribofuranosyl]adenine
  The Journal of Organic Chemistry, 1969