Concise synthesis of C2-symmetric trans-2,5-dioxymethylpyrrolidine derivatives by novel cyclization

This publication has 9 references indexed in Scilit:

• A new C2 chiral secondary amine
  The Journal of Organic Chemistry, 1988
• Concise stereoselective synthesis of (2S,4R)-4-hydroxyproline from (S)-O-benzylglycidol a novel cyclization
  Journal of the Chemical Society, Chemical Communications, 1988
• The synthesis of either (+) or (−) trans-2,5-dimethylpyrrolidine
  Tetrahedron Letters, 1987
• Asymmetric reactions using C2-symmetrically 2,5-disubstituted pyrrolidines as chiral auxiliaries.
  Journal of Synthetic Organic Chemistry, Japan, 1986
• An Efficient Synthesis of (S)-O-Benzylglycidol
  Synthesis, 1985
• A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compounds
  The Journal of Organic Chemistry, 1981
• The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
  Synthesis, 1981
• Asymmetric induction. 2. Enantioselective alkylation of cyclohexanone via a chiral enamine
  The Journal of Organic Chemistry, 1977
• Amino acids and low-molecular-weight carbohydrates of some marine red algae
  Phytochemistry, 1975