Stereospecific total synthesis of ajugarin-IV
- 1 January 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (17) , 1751-1754
- https://doi.org/10.1016/s0040-4039(00)86731-3
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Stereospecific synthesis of 9.alpha.-(acetoxymethyl)-8.alpha.,8'-epoxy-3.alpha.,4,4-trimethyl-trans-decalin-1.alpha.-ol acetate, a model for the investigation of structure-activity relationships of the insect antifeedant neoclerodanesThe Journal of Organic Chemistry, 1981
- Eine neue Synthese von CardenolidenEuropean Journal of Inorganic Chemistry, 1980
- 2-Heterosubstituted silylated ketone acetals: reagents for the preparation of .alpha.-functionalized methylketones from carboxylic acid chloridesThe Journal of Organic Chemistry, 1979
- TOTAL SYNTHESIS OF (±)-ANNONENE, A TRANS-CLERODANE DITERPENEChemistry Letters, 1979
- Selective Hydrolysis of Thioacetals with Thallium(III) NitrateSynthetic Communications, 1979
- Insect antifeedants. 1. Diels-Alders approach to the synthesis of ajugarin IThe Journal of Organic Chemistry, 1978
- Selective Thioacetal Formation of Steroid KetonesSynthesis, 1974
- The Stereochemistry of the Lithium-Ammonia Reduction of α,β-Unsaturated KetonesJournal of the American Chemical Society, 1964
- 199. Studies in the synthesis of terpenes. Part VIII. The absolute configuration of elemolJournal of the Chemical Society, 1964
- Terpenoids. XXXVII.1 The Structure of the Pentacyclic Diterpene Cafestol. On the Absolute Configuration of Diterpenes and Alkaloids of the Phyllocladene Group2Journal of the American Chemical Society, 1959