Metal salts as new catalysts for mild and efficient aminolysis of oxiranes
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (32) , 4661-4664
- https://doi.org/10.1016/s0040-4039(00)97701-3
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- A convenient preparation of β-amino alcohols from epoxides and halomagnesium alkylamidesTetrahedron Letters, 1985
- Regiospecific conversion of oxiranes, oxetanes, and lactones into difunctional nitrogen compounds via aminosilanes and aminostannanesJournal of the Chemical Society, Perkin Transactions 1, 1984
- Regiospecific Conversion of Oxiranes into Primary Alcohols via Reaction with Organotin DerivativesSynthesis, 1983
- Stereoselective total synthesis of (.+-.)-perhydrogephyrotoxin. Synthetic applications of directed 2-azonia-[3,3]-sigmatropic rearrangementsJournal of the American Chemical Society, 1980
- Carbon-carbon bond formation via directed 2-azonia-[3,3]-sigmatropic rearrangements. A new pyrrolidine synthesisJournal of the American Chemical Society, 1979
- Organic Reactions at Alumina SurfacesAngewandte Chemie International Edition in English, 1978
- Organic reactions at alumina surfaces. Mild and selective opening of epoxides by alcohols, thiols, benzeneselenol, amines, and acetic acidJournal of the American Chemical Society, 1977
- Base-induced rearrangement of epoxides. IV. Reaction of cyclohexene oxide with various lithium alkylamidesThe Journal of Organic Chemistry, 1972
- Kinetics of Reactions of Amines with Alkene OxidesBulletin of the Chemical Society of Japan, 1969
- 1,2,3-oxathiazolidines. Heterocyclic systemThe Journal of Organic Chemistry, 1969