Stereocontrolled Total Synthesis of Lipoxins As and B₅

This publication has 14 references indexed in Scilit:

• Reactions that proceed with a combination of enantiotopic group and diastereotopic face selectivity can deliver products with very high enantiomeric excess: experimental support of a mathematical model
  Journal of the American Chemical Society, 1987
• Simple and selective method for aldehydes (RCHO) .fwdarw. (E)-haloalkenes (RCH:CHX) conversion by means of a haloform-chromous chloride system
  Journal of the American Chemical Society, 1986
• Asymmetric epoxidation of allyl alcohol: efficient routes to homochiral .beta.-adrenergic blocking agents
  The Journal of Organic Chemistry, 1986
• Stereocontrolled Total Synthesis of Lipoxins B
  Synthesis, 1986
• Synthese von erythro‐D‐ und ‐L‐4‐Pententriolen; selektive Epoxyallylalkohol‐Hydrolyse unter Retention oder zweifacher Inversion (Enantiomerisierung)
  Angewandte Chemie, 1986
• Synthesis oferythro-D- and -L-4-Pentenetriols. Selective Epoxy Allyl Alcohol Hydrolysis with Retention or Twofold Inversion (Enantiomerization)
  Angewandte Chemie International Edition in English, 1986
• Stereocontrolled total synthesis of lipoxins A
  Journal of the American Chemical Society, 1985
• The regioselectivity of epoxide-opening reactions using alkynylaluminum reagents
  The Journal of Organic Chemistry, 1985
• Total synthesis of 5(S),15(S)-dihydroxy-6,13-trans-8,15-cis-eicosatetraenoic acid (5,15-diHETE) and 8(S),15(S)-dihydroxy-5,11-cis-9,13-trans-eicosatetraenoic acid (8,15-DiHETE), two novel metabolites of arachidonic acid
  Journal of the American Chemical Society, 1984
• New Synthesis of the Sex Pheromone of the Egyptian Cotton Leafworm, Spodoptera Littoralis
  Synthetic Communications, 1981