The claisen rearrangement in synthesis: acceleration of the johnson orthoester protocol en route to bicyclic lactones
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (2) , 369-380
- https://doi.org/10.1016/s0040-4020(01)80306-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Acceleration of ortho ester Claisen rearrangement by a commercial microwave ovenJournal of the Chemical Society, Perkin Transactions 1, 1992
- APPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY. A REVIEWOrganic Preparations and Procedures International, 1991
- Clay catalyzed rearrangement of substituted allyl phenyl ethers: Synthesis of ortho-allyl phenols, chromans and coumaransTetrahedron Letters, 1990
- STEREOCONTROLLED IODOLACTONIZATION OF ACYCLIC OLEFINIC ACIDS: THE trans AND cis ISOMERS OF 4,5-DIHYDRO-5-IODOMETHYL-4-PHENYL-2(3H)-FURANONEOrganic Syntheses, 1986
- Application of commercial microwave ovens to organic synthesis.Tetrahedron Letters, 1986
- Lanthanoids in organic synthesis. 6. Reduction of .alpha.-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspectsJournal of the American Chemical Society, 1981
- Phenylselenolactonization. An extremely mild and synthetically useful cyclization processJournal of the American Chemical Society, 1977
- Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squaleneJournal of the American Chemical Society, 1970