Stereocontrolled construction of a spiro fused bicyclo[2.2.2]Octane ring system by the intramolecular double michael reaction
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (20) , 2167-2170
- https://doi.org/10.1016/s0040-4039(01)81189-8
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Biogenetic-type total synthesis of (.+-.)-aphidicolinJournal of the American Chemical Society, 1983
- On the Construction of the C/D‐Ring Systems of Aphidicolin and Stemodin: a Regio‐ and Stereospecific Synthesis of 17‐Noraphidicolaii‐16 one and 17‐Norstemodan‐16‐one Preliminary CommunicationHelvetica Chimica Acta, 1982
- Total synthesis of (.+-.)-maritimolJournal of the American Chemical Society, 1981
- A total synthesis of racemic eriolaninJournal of the American Chemical Society, 1981
- Synthetic Approach to Diterpene Alkaloids — A Simple and Novel Synthesis of the A, B, C and D Ring Part from 1-Benzyl-1,2,3,4-tetrahydroisoquinolineHETEROCYCLES, 1981
- A total synthesis of (±)-stemarin, a diterpenoid with a unique bicyclic C/D ring SystemCanadian Journal of Chemistry, 1980
- One-step synthesis of tricyclo[5.2.2.02,6]undecane derivatives: precursors to pleuromutilinThe Journal of Organic Chemistry, 1980
- Simple Method for the Esterification of Carboxylic AcidsAngewandte Chemie International Edition in English, 1978
- A Stereospecific Total Synthesis of ChasmanineHETEROCYCLES, 1977
- The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formationJournal of the American Chemical Society, 1976