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DC Field | Value | Language |
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dc.contributor.author | F. Louafi, J.-P. Hurvois, A.Chibani | - |
dc.date.accessioned | 2013-12-19T11:42:10Z | - |
dc.date.available | 2013-12-19T11:42:10Z | - |
dc.date.issued | 2013-12-19 | - |
dc.identifier.issn | saf | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2502 | - |
dc.description | 1st International Days of Organometallic Chemistry and Catalysis JICOC Ouargla, February 06- 09, 2012 | en_US |
dc.description.abstract | Due to widespread occurrence in nature and marked physiological action, 1- substituted tetrahydroisoquinoline alkaloids have long offered intensive targets for synthesis.1 in this regard, the enantioselective construction of 1-substituted tetrahydroisoquinoline has attracted growing attention in the last decade.2 We describe here in this communication a novel asymmetric approach to the synthesis of 1- substituted tetrahydroisoquinoline by deprotonation of an -amino nitrile and alkylation of the resulting carbanion followed by asymmetric reduction3 | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartofseries | 2012; | - |
dc.subject | Asymmetric synthesis | en_US |
dc.subject | tetra-hydroisoquinolines | en_US |
dc.subject | alkaloids | en_US |
dc.title | Asymmetric synthesis of 1-substituted tetra-hydroisoquinolines alkaloids | en_US |
dc.type | Article | en_US |
Appears in Collections: | 1. Faculté des mathématiques et des sciences de la matière |
Files in This Item:
File | Description | Size | Format | |
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F. Louafi.pdf | 160,51 kB | Adobe PDF | View/Open |
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