Synthesis of Enantiomerically Pure 1,7-Dioxaspiro[5.5]undecanes, Pheromone Components of the Olive Fly (Dacus oleae)

This publication has 14 references indexed in Scilit:

• Pheromone Synthesis, LXIV. Synthesis of the Enantiomers of 2‐Methyl‐1,7‐dioxaspiro[5.6]‐dodecane, a Component of the Volatile Secretion from the Mandibular Glands of Andrena haemorrhoa F.
  European Journal of Organic Chemistry, 1984
• Chirale Bausteine aus Kohlenhydraten, IX Synthese enantiomerer 2,8‐Dimethyl‐1,7‐dioxaspiro‐[5.5]undecan‐4‐ole, Komponenten aus dem Pheromonbouquet von Andrena wilkella
  European Journal of Organic Chemistry, 1983
• Chirale Bausteine aus Kohlenhydraten, VI. Synthese von (2R,5RS)‐ und (2S,5RS)‐2‐Ethyl‐1,6‐dioxaspiro‐[4.4]nonan (Chalcogran) aus D‐Glucose
  European Journal of Organic Chemistry, 1982
• Synthesis of optically active 2s-, and 7s-methyl-1.6-dioxa-spiro[4.5] decane, the pheromone components of Paravespula vulgaris (L.), from S-ethyl lactate.
  Tetrahedron Letters, 1981
• Synthesis of three stereoisomeric forms of 2,8-dimethyl-1,7-dioxaspiro[5.5]undecane, the main component of the cephalic secretion of andrena wilkella
  Tetrahedron, 1981
• Synthese optisch aktiver 2‐Methyl‐ und 2‐Äthyl‐1, 6‐dioxaspiro [4.4]‐nonan‐ und ‐[4.5]decan‐Pheromone aus einem gemeinsamen chiralen Vorläufer
  Helvetica Chimica Acta, 1980
• Enantiomer resolution of spiroketals
  The Science of Nature, 1980
• Mass-spectrometric fragmentation of alkyl-1,6-dioxaspiro[4.5]decanes
  The Science of Nature, 1979
• Synthesis of Optically Active 2-Ethyl-1,6-dioxaspiro[4.4]nonane(Chalcogran), the Principal Aggrega-tion Pheromone of Pityogenes Chalcographus (L.)
  HETEROCYCLES, 1978
• Elements of stereoisomerism and prostereoismerism
  The Journal of Organic Chemistry, 1971