Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives
The reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated c...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Beilstein-Institut
2012-12-01
|
| Series: | Beilstein Journal of Organic Chemistry |
| Subjects: | |
| Online Access: | https://doi.org/10.3762/bjoc.8.244 |
| _version_ | 1818865733952602112 |
|---|---|
| author | Ishmael B. Masesane Zelalem Yibralign Desta |
| author_facet | Ishmael B. Masesane Zelalem Yibralign Desta |
| author_sort | Ishmael B. Masesane |
| collection | DOAJ |
| description | The reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated compounds. |
| first_indexed | 2024-12-19T10:52:15Z |
| format | Article |
| id | doaj.art-8e8a2f38974948f38829abf1a24babd7 |
| institution | Directory Open Access Journal |
| issn | 1860-5397 |
| language | English |
| last_indexed | 2024-12-19T10:52:15Z |
| publishDate | 2012-12-01 |
| publisher | Beilstein-Institut |
| record_format | Article |
| series | Beilstein Journal of Organic Chemistry |
| spelling | doaj.art-8e8a2f38974948f38829abf1a24babd72022-12-21T20:24:57ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972012-12-01812166217510.3762/bjoc.8.2441860-5397-8-244Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivativesIshmael B. Masesane0Zelalem Yibralign Desta1Department of Chemistry, University of Botswana, Private Bag 00704, Gaborone, BotswanaDepartment of Chemistry, University of Botswana, Private Bag 00704, Gaborone, BotswanaThe reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated compounds.https://doi.org/10.3762/bjoc.8.244acetophenonechromaneenolatesmalononitrileMichael additionsalicylaldehyde |
| spellingShingle | Ishmael B. Masesane Zelalem Yibralign Desta Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives Beilstein Journal of Organic Chemistry acetophenone chromane enolates malononitrile Michael addition salicylaldehyde |
| title | Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives |
| title_full | Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives |
| title_fullStr | Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives |
| title_full_unstemmed | Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives |
| title_short | Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives |
| title_sort | reactions of salicylaldehyde and enolates or their equivalents versatile synthetic routes to chromane derivatives |
| topic | acetophenone chromane enolates malononitrile Michael addition salicylaldehyde |
| url | https://doi.org/10.3762/bjoc.8.244 |
| work_keys_str_mv | AT ishmaelbmasesane reactionsofsalicylaldehydeandenolatesortheirequivalentsversatilesyntheticroutestochromanederivatives AT zelalemyibraligndesta reactionsofsalicylaldehydeandenolatesortheirequivalentsversatilesyntheticroutestochromanederivatives |