Synthetic Studies on the Ingenane Diterpenes. Direct Conversion of the out,out-Bicyclo[4.4.1]undecane System into a Highly Strained In,out Stereoisomer
- 15 November 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (23) , 7992-7993
- https://doi.org/10.1021/jo961714o
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- A Unified Entry into the Ingenane, Tigliane, and Taxane Ring SystemsThe Journal of Organic Chemistry, 1995
- On the Protein Kinase C Pharmacophore: Synthesis and Biological Activity of 4-Hydroxylated Analogs of IngenolSynlett, 1995
- Inside-outside stereoisomerism. VII. Methodology for the Synthesis of 3-Oxygenated Ingenanes. The First Ingenol Analogs with High Affinity for Protein Kinase CThe Journal of Organic Chemistry, 1995
- Inside-Outside Stereoisomerism. 6.+ Synthesis of trans-Bicyclo[4.4.1]undecan-11-one and the First Stereoselective Construction of the Tricyclic Nucleus of the Ring System of the Ingenane DiterpenesJournal of the American Chemical Society, 1994
- Transition metal promoted higher-order cycloaddition reactions in organic synthesisAccounts of Chemical Research, 1993
- Stereoselective construction of the complete ingenane ring systemThe Journal of Organic Chemistry, 1993
- A solution to the in,out-bicyclo[4.4.1]undecan-7-one problem inherent in ingenane total synthesisJournal of the American Chemical Society, 1988
- Medium-ring bicyclic compounds and intrabridgehead chemistryAccounts of Chemical Research, 1983
- Relationship of the anionic behavior of unsaturated medium-ring alcohols to structure. Generation and antarafacial cyclization of coiled 8.pi.-electron carbanionsJournal of the American Chemical Society, 1982
- Base-Catalyzed lsomerization of Epoxides. II. Preparation of 3-Hydroxycyclooctene from Cyclooctene OxideSynthesis, 1972