Clay montmorillonite-catalyzed regioselective addition of silyl ketene acetals to pyridine derivatives: synthesis of N-silyldihydropyridines
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (6) , 747-750
- https://doi.org/10.1016/s0040-4039(01)80299-9
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Clay Montmorillonite: An Efficient, Heterogeneous Catalyst for Michael Reactions of Silyl Ketene Acetals and Silyl Enol Ethers with α,β-Unsaturated Carbonyl CompoundsBulletin of the Chemical Society of Japan, 1988
- New Application of Solid Acid to Carbon–Carbon Bond Formation Reactions: Clay Montmorillonite-Catalyzed Aldol Reactions of Silyl Enol Ethers with Aldehydes and AcetalsBulletin of the Chemical Society of Japan, 1988
- Regioselective synthesis of 4-(2-oxoalkyl)pyridines via 1,4-dihydro-pyridine derivatives using silyl enol ethers and pyridinium saltsTetrahedron Letters, 1983
- Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridinesThe Journal of Organic Chemistry, 1982
- Regioselective synthesis of 4-alkylpyridines via 1,4-dihydropyridine derivatives from pyridineTetrahedron Letters, 1982
- Reaction of Cuprate Reagents with Pyridine in the Presence of Chloroformate. A Novel Synthesis of 1,4-Dihydropyridine DerivativesCanadian Journal of Chemistry, 1974