Pyridinium dichromate-induced 1,3-oxidative rearrangements of enynols
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (10), 1069-1072
- https://doi.org/10.1016/s0040-4039(00)95913-6
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Origins of regio- and stereoselectivity in additions of phenylselenenyl chloride to allylic alcohols and the applicability of these additions to a simple 1,3-enone transposition sequenceThe Journal of Organic Chemistry, 1982
- Acidities of sulfoximines and related oxosulfonium cations. Cyclopropyl effects and structures of .alpha.-sulfonyl-type carbanionsThe Journal of Organic Chemistry, 1980
- Direct oxidation of tertiary allylic alcohols. A simple and effective method for alkylative carbonyl transpositionThe Journal of Organic Chemistry, 1977
- Oxidative rearrangements of tertiary and some secondary allylic alcohols with chromium(VI) reagents. A new method for 1,3-functional group transposition and forming mixed aldol productsThe Journal of Organic Chemistry, 1977
- New stereocontrolled approach to spirosesquiterpenes. Synthesis of acorenone BJournal of the American Chemical Society, 1975
- Method for catalytic dehalogenations via trialkyltin hydridesThe Journal of Organic Chemistry, 1975
- New synthetic methods. 1,3-Alkylative carbonyl transpositionJournal of the American Chemical Society, 1975
- Regiospecific alkylation of cyclic .beta.-diketone enol ethers. General synthesis of 4-alkylcyclohexenonesThe Journal of Organic Chemistry, 1973
- Selenium dioxide oxidation of olefins. Evidence for the intermediacy of allylseleninic acidsJournal of the American Chemical Society, 1972
- Self-immolative asymmetric synthesis in the allylic rearrangement of an optically active amine oxideJournal of the Chemical Society D: Chemical Communications, 1970