Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspirol[5.5]undecane and 3-hydroxy-1,7-dioxaspiroi[5.5]undecane

This publication has 20 references indexed in Scilit:

• Doppelt und dreifach funktionalisierte, enantiomerenreine C₄‐Synthesebausteine aus β‐Hydroxybuttersäure, Äpfelsäure und Weinsäure
  Helvetica Chimica Acta, 1981
• 1,7-Dioxaspiro[5.5]undecanes. An excellent system for the study of stereoelectronic effects (anomeric and exo-anomeric effects) in acetals
  Canadian Journal of Chemistry, 1981
• Pheromonsynthesen ‐ Modellreaktionen zur Synthese von Polyether‐Antibiotika
  European Journal of Inorganic Chemistry, 1981
• The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
  Synthesis, 1981
• Bestimmung der relativen Konfiguration bei Spiroacetalen durch ¹H‐ und ¹³C‐NMR‐Spektroskopie
  European Journal of Inorganic Chemistry, 1980
• Identification and synthesis of the major sex pheromone of the olive fly (Dacus oleae)
  Journal of the Chemical Society, Chemical Communications, 1980
• 1,3-Dithianes Derived from 1,2-Dimethyl-4,5-bis-[mercaptomethyl]benzene as Synthons for the Synthesis of Aldehydes and Ketones
  Synthesis, 1975
• Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
  Journal of the American Chemical Society, 1973
• A Convenient Method for Hydrolysis of 1,3-Dithiane Derivatives Using Cupric Chloride
  Bulletin of the Chemical Society of Japan, 1972
• N,N,N',N'-Tetramethylphosphorodiamidate group. Useful function for the protection or reductive deoxygenation of alcohols and ketones
  Journal of the American Chemical Society, 1972