EFFICIENT SYNTHESIS OF SECONDARY CARBOXAMIDES WITH ω-SUBSTITUTED ETHYL AND PROPYL GROUPS ON NITROGEN ATOM BY NUCLEOPHILIC RING OPENING OF CYCLIC IMIDATES
- 5 July 1984
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 13 (7), 1243-1246
- https://doi.org/10.1246/cl.1984.1243
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Stereocontrolled total synthesis of (+)-actinobolin by an intramolecular Diels-Alder reaction of a chiral Z-diene derived from L-threonineJournal of the American Chemical Society, 1984
- Stereospecific synthesis of retronecine by imidate methylide cycloadditionJournal of the American Chemical Society, 1980
- The Synthetic Utility of 2‐OxazolinesAngewandte Chemie International Edition in English, 1976
- Die Nützlichkeit der 2‐Oxazoline in der SyntheseAngewandte Chemie, 1976
- Methods in alkaloid synthesis. Imino ethers as donors in the Michael reactionJournal of the American Chemical Society, 1975
- Stereoelectronic control in the cleavage of tetrahedral intermediates in the hydrolysis of esters and amidesTetrahedron, 1975
- Die Reaktionsweise ambidenter KationenAngewandte Chemie, 1964
- Action of Grignard Reagents on Heterocyclic Compounds. I. Action of Grignard Reagents on Unsaturated AzlactonesThe Journal of Organic Chemistry, 1960
- OXAZOLINE RING-OPENINGThe Journal of Organic Chemistry, 1950
- OXAZOLINESThe Journal of Organic Chemistry, 1949