A new free radical-based method for the synthesis of spiroannulated medium rings
- 2 June 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (23), 3285-3288
- https://doi.org/10.1016/s0040-4039(00)92068-9
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Free radical ring expansion of fused cyclobutanones: a new ring expansion annulation stratagemJournal of the American Chemical Society, 1991
- The magnesium complexes of 1,2-dimethylenecycloalkanes: a new method for a one-step spiroannelationTetrahedron Letters, 1991
- General synthesis of 1-oxaspiro[4.5]decan-2-ones and 1-oxaspiro[4.5]decanes from 5-methylene-2(5H)-furanoneThe Journal of Organic Chemistry, 1991
- A route to linear, bridged, or spiro polycyclic compounds: sequential use of the intermolecular Diels-Alder reaction and radical cyclizationThe Journal of Organic Chemistry, 1990
- Organobis(cuprates): a new class of reagents and method for spiroannelationJournal of the American Chemical Society, 1988
- Vitamin B12-mediated electrochemical reactions in the synthesis of natural productsPublished by Walter de Gruyter GmbH ,1987
- 2‐Vinylcyclobutanones by Cycloaddition of Vinylketenes to Simple OlefinsHelvetica Chimica Acta, 1983
- Hetero-Diels-Alder-Reaktionen zwischen elektronenreichen 1,3-Dienen und 1,2, 3-Tricarbonyl-VerbindungenSynthesis, 1983
- Palladium-catalyzed preparation of carbon and oxygen spirocyclesThe Journal of Organic Chemistry, 1982
- 1.2.3‐Tricarbonylverbindungen, V. Hydratbildende cyclische 1.2.3‐Tricarbonylverbindungen als Dienophile in Diels‐Alder‐ReaktionenEuropean Journal of Inorganic Chemistry, 1971