Synthesis of cyclic ethers from copper carbenoids by formation and rearrangement of oxonium ylides
- 1 July 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (27) , 4385-4388
- https://doi.org/10.1016/s0040-4039(00)79359-2
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Diastereoselective synthesis of 2,5-dialkyl tetrahydrofuran-3-ones by a copper-catalysed tandem carbenoid insertion and ylide rearrangement reactionTetrahedron Letters, 1992
- The Stevens [1,2]-shift of oxonium ylides: a route to substituted tetrahydrofuranonesThe Journal of Organic Chemistry, 1992
- Synthesis of medium ring ethers. Part 2. Synthesis of the fully saturated carbon skeleton of Laurencia non-terpenoid ether metabolites containing seven-, eight- and nine-membered ringsJournal of the Chemical Society, Perkin Transactions 1, 1992
- Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairsChemical Reviews, 1991
- Rhodium (II) catalyzed reactions of diazo-carbonyl compoundsTetrahedron, 1991
- Rhodium acetate catalyzes the addition of carbenoids α- to ether oxygensTetrahedron Letters, 1989
- A Gentle Method for the Preparation of a Variety of Ylides (As, Sb, Bi, S, Te, Thiouronium) from Diazo CompoundsSynthesis, 1988
- Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural productsTetrahedron, 1987
- Generation and rearrangements of oxonium ylidesJournal of the American Chemical Society, 1986
- Intramolecular generation and [2,3]-sigmatropic rearrangement of oxonium ylidesJournal of the American Chemical Society, 1986