Diastereoselektive Synthese von Spiro[4.5]decanonen durch intramolekulare Sakurai‐Reaktionen
- 1 April 1984
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 96 (4) , 292-293
- https://doi.org/10.1002/ange.19840960411
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Stereochemistry of the Sakurai reaction. Additions to cyclohexenones and cycloheptenonesJournal of the American Chemical Society, 1983
- Total Synthesis of (±)‐α‐Acoradiene via Intramolecular Photoaddition and Reductive Cyclobutane CleavageHelvetica Chimica Acta, 1983
- Allylsilane initiated garbocyclizationsTetrahedron Letters, 1983
- Chemoselectivity in the conjugate addition of allylsilane to Michael acceptorsTetrahedron Letters, 1983
- Total synthesis of (±)-lubimin and (±)-oxylubiminJournal of the Chemical Society, Chemical Communications, 1982
- A Stereoselective Approach to the Spiro [4, 5]decane System via Intramolecular Photocycloaddition and Reductive Fragmentation. Preliminary communicationHelvetica Chimica Acta, 1981
- Chemistry of organosilicon compounds. 99. Conjugate addition of allylsilanes to .alpha.,.beta.-enones. A New method of stereoselective introduction of the angular allyl group in fused cyclic .alpha.,.beta.-enonesJournal of the American Chemical Society, 1977