The regioselective S → C and S → N allylic rearrangement of S-allylthioimidate
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (42) , 4245-4248
- https://doi.org/10.1016/s0040-4039(01)82116-x
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- A convenient method for the selective reduction of amides to aminesTetrahedron Letters, 1980
- Stereoselective generation of Z-enolates of thioamides: its application to diastereoselective aldol condensations and thio-Claisen rearrangementsJournal of the American Chemical Society, 1980
- Thio-Claisen and Cope rearrangements. A general method for the synthesis of .alpha.,.beta.,.alpha.,.zeta.-unsaturated thioamidesJournal of the American Chemical Society, 1980
- 1,4-Addition reactions of lithium enolates to .alpha.,.beta.-unsaturated thioamidesJournal of the American Chemical Society, 1979
- 1,4-Addition reaction of organolithium and -magnesium compounds to .alpha.,.beta.-unsaturated thioamidesJournal of the American Chemical Society, 1978
- Stereoselective coupling reaction of thioamides via a dithia-Cope rearrangementJournal of the American Chemical Society, 1978
- A new entry into the synthesis of the nine-membered indole alkaloids related to cleavamine. A stereospecific synthesis of (dl)-4.alpha.-dihydrocleavamine and (dl)-quebrachamine via the thio-Claisen rearrangementJournal of the American Chemical Society, 1976
- Hetero-Cope-Umlagerungen mit dipolaren ZwischenproduktenAngewandte Chemie, 1976
- Synthetic studies on histrionicotoxins. II. Practical synthetic route to (+-)-perhydro- and (+-)-octahydrohistrionicotoxinThe Journal of Organic Chemistry, 1975
- Sulfidkontraktion via alkylative Kupplung: Eine methode zur darstellung von β‐dicarbonylderivaten. Über synthetische methoden, 1. MitteilungHelvetica Chimica Acta, 1971