Mechanism of the photochemical substitution of 6-membered ring monoazaaromatic compounds by methanol in neutral and HCl acidified medium
- 1 January 1975
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 31 (18), 2255-2261
- https://doi.org/10.1016/0040-4020(75)80224-9
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Photochemical Studies. XVI. Second Moment Analysis of the Electron Spin Resonance Spectra of Radicals Formed by Ultraviolet Irradiation of 9-Phenylacridine and of AcridineCanadian Journal of Chemistry, 1973
- Photochemistry of aza aromatics. Identification of the reactive intermediate in the photoreduction of acridineJournal of the American Chemical Society, 1971
- Etudes photochimiques VIITetrahedron, 1971
- Etudes photochimiques—VITetrahedron, 1971
- Etudes photochimiques—VIIITetrahedron, 1971
- Nitrogen photochemistry. IV. Photochemical reduction of the cinchona alkaloids, quinine, quinidine, cinchonidine, and cinchonineThe Journal of Organic Chemistry, 1970
- Photochemistry of n-heterocycles. V. Photochemistry of quinoline and some substituted quinoline derivativesJournal of the American Chemical Society, 1970
- Photoalkylation of pyridine with methanolJournal of the Chemical Society D: Chemical Communications, 1970
- A new photoreduction on quinoline alkaloidsTetrahedron Letters, 1969
- Imine photoalkylations. Papaverine, phenanthridine, and a general mechanismThe Journal of Organic Chemistry, 1968