Sequential Ugi reaction/base-induced ring closing/IAAC protocol toward triazolobenzodiazepine-fused diketopiperazines and hydantoins.

scientific article

Sequential Ugi reaction/base-induced ring closing/IAAC protocol toward triazolobenzodiazepine-fused diketopiperazines and hydantoins. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3762/BJOC.14.49
P932PMC publication ID5870159
P698PubMed publication ID29623124

P50authorJubi JohnQ50222211
Robby VroemansQ53695353
Luc Van MeerveltQ58050016
Wim DehaenQ66724685
Jonas WintersQ88287753
P2093author name stringJoice Thomas
Jeroen Jacobs
Fante Bamba
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P304page(s)626-633
P577publication date2018-03-14
P1433published inBeilstein Journal of Organic ChemistryQ2894008
P1476titleSequential Ugi reaction/base-induced ring closing/IAAC protocol toward triazolobenzodiazepine-fused diketopiperazines and hydantoins
P478volume14

Reverse relations

cites work (P2860)
Q58578763Assembly of fully substituted triazolochromenes via a novel multicomponent reaction or mechanochemical synthesis
Q64269467One-Pot Synthesis of Triazolobenzodiazepines Through Decarboxylative [3 + 2] Cycloaddition of Nonstabilized Azomethine Ylides and Cu-Free Click Reactions
Q97542697One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions