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Title: | Sequential Ugi Reaction/Base-induced Ring Closing/IAAC Protocol Toward Triazolobenzodiazepine-fused Diketopiperazines and Hydantoins |
Authors: | Robby, V Bamba, F Jonas, W Joice, T Jeroen, J Meervelt, L V Jubi John Wim, D |
Keywords: | benzodiazepine 2,5-diketopiperazine hydantoin intramolecular azide–alkyne cycloaddition Ugi reaction |
Issue Date: | 14-Mar-2018 |
Publisher: | Beilstein-Institut |
Citation: | Beilstein Journal of Organic Chemistry, 14:626-633 |
Abstract: | A practical three-step protocol for the assembly of triazolobenzodiazepine-fused diketopiperazines and hydantoins has been developed. The synthesis of these tetracyclic ring systems was initiated by an Ugi reaction, which brought together all necessary functionalities for further transformations. The Ugi adducts were then subjected to a base-induced ring closing and an intramolecular azide–alkyne cycloaddition reaction in succession to obtain highly fused benzodiazepine frameworks. |
URI: | http://10.10.100.66:8080/xmlui/handle/123456789/3090 |
Appears in Collections: | 2018 |
Files in This Item:
File | Description | Size | Format | |
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Sequential Ugi reaction - Robby V - Beilstein Journal of Organic Chemistry.pdf Restricted Access | 750.46 kB | Adobe PDF | View/Open Request a copy |
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