Synthesis in the diterpene alkaloid series - I the stereospecific synthesis of an intermediate and its identification with a natural degradation product
- 31 December 1962
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 3 (19) , 869-872
- https://doi.org/10.1016/s0040-4039(00)71737-0
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A NEW PHOTOCHEMICAL REACTION: THE STRUCTURE AND ABSOLUTE STEREOCHEMISTRY OF ATISINECanadian Journal of Chemistry, 1962
- A Stereospecific Route to the Dehydroabietic Acid Configuration1Journal of the American Chemical Society, 1961
- The structure of ajaconineTetrahedron, 1961
- On the absolute congifuration of the diterpene alkaloids related to veatchine and atisineTetrahedron Letters, 1961
- THE CORRELATION OF THE ATISINE AND VEATCHINE SERIES OF DITERPENE ALKALOIDS1Journal of the American Chemical Society, 1960
- A NEW RING ENLARGEMENT SEQUENCEJournal of the American Chemical Society, 1956
- A NEW ALKYLATION OF CARBONYL COMPOUNDS. II1Journal of the American Chemical Society, 1956
- The basicity and steric configuration of the diterpene alkaloids veatchine and atisineCellular and Molecular Life Sciences, 1955
- Garrya Alkaloids. III. The Skeletal Structure of the Garrya AlkaloidsJournal of the American Chemical Society, 1954
- 396. Experiments on the synthesis of substances related to the sterols. Part XLVIII. Synthesis of a tricyclic degradation product of cholesterolJournal of the Chemical Society, 1949