Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3090
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 SizeFormat 
Sequential Ugi reaction - Robby V - Beilstein Journal of Organic Chemistry.pdf
  Restricted Access
750.46 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.