A Rare Acid-Promoted Elimination of O-Methyl Oximes: A Practical Synthesis of 3-Cyano-4-benzopyrones
- 22 October 1999
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (23) , 8736-8740
- https://doi.org/10.1021/jo991031j
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Sequential 1,2-Addition−Electrocyclic Ring Closures Involving Acyclic α,β-Unsaturated Iminiums: A Formal [3 + 3] Cycloaddition Strategy to Unique Pyranyl SpirocyclesThe Journal of Organic Chemistry, 1999
- Formaldehyde Dialkylhydrazones as Neutral Formyl Anion and Cyanide Equivalents: Nucleophilic Addition to Conjugated EnonesThe Journal of Organic Chemistry, 1997
- The Anti-HIV Activity and Mechanisms of Action of Pure Compounds Isolated fromRosa damascenaBiochemical and Biophysical Research Communications, 1996
- Conversion of Formyl into Cyano groups in kojic acid derivatives and analoguesAdvanced Synthesis & Catalysis, 1996
- Synthesis of Milrinone, a Cardiotonic AgentHETEROCYCLES, 1990
- Total synthesis of (.+-.)-forskolinJournal of the American Chemical Society, 1988
- Oral Tetrahydroaminoacridine in Long-Term Treatment of Senile Dementia, Alzheimer TypeNew England Journal of Medicine, 1986
- Studies on Antianaphylactic Agents. 7. Synthesis of Antiallergic 5-Oxo-5H-[1]benzopyrano[2,3-b]pyridinesJournal of Medicinal Chemistry, 1985
- Untersuchungen an 1,3-Dicarbonyl-Verbindungen, 21. Mitt. 3-Acyl-4,5-dihydro-4-oxo-indeno[1,2-b]pyraneArchiv der Pharmazie, 1984
- N-amination and subsequent oxidation of some fused imidazoles and triazolesJournal of the Chemical Society, Perkin Transactions 1, 1976