A suite of odd and even carbon-numbered spiroacetals in Bactrocera latifrons. Synthesis and stereochemistry

This publication has 7 references indexed in Scilit:

• Chemistry of fruit flies
  Chemical Reviews, 1995
• An Efficient Synthesis of Enantiomerically Pure (R)-(2-Benzyloxyethyl)oxirane from (S)-Aspartic Acid
  Synthesis, 1992
• An (S)-(+)-lactic acid route to (2S,6R,8S)-2,8 dimethyl-1,7-dioxaspiro[5,5]undecane and (2S,6R,8S)-2-ethyl-8-methyl-1,7-dioxaspiro[5,5]undecane and demonstration of their presence in the rectal glandular secretion of Bactrocera nigrotibialis(Perkins)
  Journal of the Chemical Society, Perkin Transactions 1, 1990
• Chemo- and Regioselective Reduction of Epoxides with Sodium Borohydride in Mixed Solvent Containing Methanol
  Bulletin of the Chemical Society of Japan, 1987
• Optical Rotatory Dispersion of Spiroacetals
  European Journal of Organic Chemistry, 1987
• Spiroacetals in rectal gland secretions of australasian fruit fly species
  Journal of the Chemical Society, Chemical Communications, 1986
• Enhancement of optical purity of a product by removing unwanted diastereomers in the course of a chiral synthesis: new synthesis of the stereoisomers of 2,8-dimethyl-1,7-dioxaspiro[5.5]undecane, the pheromone of
  Tetrahedron, 1985