1. The stereospecific total synthesis of d1-8β-carbomethoxy-13-oxopodocarpane, a degradation product of phyllocladene
2. “The Chemistry of Heterocyclic Compounds,”;Klingsberg,1962
3. In a paper4 that has often been overlooked as a contribution to the study of Claisen rearrangement of pyridyl and quinolyl allyl ethers (largely because it emphasized in its title the synthesis of antimalarial compounds) the allyl ethers were obtained by reacting hydroxyquinolines and hydroxypyridines with allyl bromide in acetone in the presence of potassium carbonate as base. None of the products from such a reaction was examined to verify if they were N-allyl or O-allyl derivatives. These were then subjected to rearrangement in refluxing alpha methylnaphthalene and the products of rearrangement were assumed to be the corresponding C-allylhydroxypyridines and quinolines.
4. Über einen neuen, gegen Vogelmalaria wirksamen Verbindungstypus