Zonouzi, A. and Izakian, Z. and Ng, S.W. (2016) Novel domino procedures for the synthesis of chromene derivatives and their isomerization. Molecular Diversity, 20 (3). pp. 627-638. ISSN 1381-1991, DOI https://doi.org/10.1007/s11030-016-9664-0.
Full text not available from this repository.Abstract
Novel tricyclic keto diesters have been synthesized by a one-pot three-component procedure via DABCO-catalyzed domino Knoevenagel–Michael addition reactions. Also, an efficient four-component reaction for the synthesis of another new group of tricyclic keto diesters has been developed via domino Knoevenagel-intramolecular oxo-Diels–Alder reactions. A selective thermal isomerization of the synthesized chromenes to fumarates is also described. X-ray analyses confirm unambiguously the structures of the products.
| Item Type: | Article |
|---|---|
| Funders: | UNSPECIFIED |
| Uncontrolled Keywords: | Domino reaction; Michael addition; Oxo-Diels–Alder; Chromene; Isomerization; DABCO; Iminolactone; MCRs |
| Subjects: | Q Science > Q Science (General) Q Science > QD Chemistry |
| Divisions: | Faculty of Science > Department of Chemistry |
| Depositing User: | Ms. Juhaida Abd Rahim |
| Date Deposited: | 14 May 2018 07:43 |
| Last Modified: | 14 May 2018 07:43 |
| URI: | http://eprints.um.edu.my/id/eprint/18658 |
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