Synthesis and Thermolysis of Cycloalkenyl Azides and Iminophosphoranes Aldehydes: A New Pathway to Bisannelated Pyridines
- 1 September 1988
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 18 (13) , 1475-1482
- https://doi.org/10.1080/00397918808081303
Abstract
Nucleophilic substitution on vinyl halides usually occurs when these compounds possess an electron withdrawing group at the D position as well as a good leaving group at the Q position Thus D-chlorovinyl ketones are suitable starting materials for the synthesis of D-azidovinyl ketones' Nesmeyanov and Rybuiskaya2 found that this substitution proceeds with the retention of configuration regarding the C=C bond Consequently, trans-β-halovinyl ketones yield the corresponding trans-D-azido ketones, but very few cis-D-azidovinyl ketone or aldehyde are described3 These latter Isomers have been reported to be unstable and to decompose spontaneously to isoxazoles2 In the case of the cycloalkenyl series β-azidovinyl ketones were only suggested as reaction Intermediatesl,3Keywords
This publication has 4 references indexed in Scilit:
- A New Versatile Synthesis of Isoquinolines by Condensation of Iminophosphoranes witho-PhthalaldehydeSynthetic Communications, 1987
- A useful, regiospecific synthesis of isoxazolesThe Journal of Organic Chemistry, 1978
- Preparation and properties of annelated pyridinesThe Journal of Organic Chemistry, 1977
- β-KetovinylationRussian Chemical Reviews, 1969