Synthesis of indolines from N‐allylarylamines
- 1 June 1976
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 13 (3) , 555-560
- https://doi.org/10.1002/jhet.5570130326
Abstract
A novel method of synthesis of nitrogen heterocycles is described. The acidic rearrangement of N‐allylanilines gives 2‐allylanilines which lead to indolines by photocyclization.Keywords
This publication has 8 references indexed in Scilit:
- Photochemical Cyclization of Allylated Anisole and N‐Alkyl Aniline Derivatives. Preliminary communicationHelvetica Chimica Acta, 1975
- Transposition d'amines β,γ-ethyleniques vii prototropie et transposition type claisen d'amines cycleniquesTetrahedron Letters, 1974
- Zinkchloridkatalysierte, thermische Umlagerungen von N‐Allyl in C‐Allyl‐aniline; ladungsinduzierte, aromatische Amino‐Claisen‐UmlagerungenHelvetica Chimica Acta, 1973
- Influence d'une substitution en α de l'azote sur le rearrangement photochimique des amines aromatiques N-allyliquesTetrahedron Letters, 1971
- Hydrogenolysis by Metal Hydrides. III. Hydrogenolysis of Alkylallylarylamines by Lithium Aluminum Hydride1The Journal of Organic Chemistry, 1961
- Indoles. II.1a,1b The Acid-catalyzed Rearrangement of N-2-AlkenylanilinesJournal of the American Chemical Society, 1961
- Unsaturated Aromatic Amines; a Novel Synthesis of IndolesJournal of the American Chemical Society, 1958
- Decomposition of Allylanilines in the Presence of Zinc Chloride*The Journal of Organic Chemistry, 1957