[PDF][PDF] Oxindole as starting material in organic synthesis

GM Ziarani, P Gholamzadeh, N Lashgari, P Hajiabbasi - Arkivoc, 2013 - academia.edu
This review highlights the advances in the use of oxindole as starting material in the
synthesis of various organic compounds and drugs. The reactions can be performed on …

Barbituric acids in organic transformations, an outlook to the reaction media

K Nikoofar, Z Khademi - Mini-Reviews in Organic Chemistry, 2017 - ingentaconnect.com
Barbituric acid (pyrimidine-2, 4, 6 (1H, 3H, 5H)-trione) as odourless white crystals has been
prepared in 1864. Due to the acidity of the CH2 group, the pyrimidine ring of barbituric acid …

An efficient synthesis of 1, 3-dimethyl-5-(2-phenyl-4 H-chromen-4-ylidene) pyrimidine-2, 4, 6 (1 H, 3 H, 5 H)-triones and investigation of their interactions with β …

N Sepay, S Mallik, C Guha, AK Mallik - RSC advances, 2016 - pubs.rsc.org
An efficient method for synthesis of 1, 3-dimethyl-5-(2-phenyl-4H-chromen-4-ylidene)
pyrimidine-2, 4, 6 (1H, 3H, 5H)-triones has been developed by treatment of 2 …

Regioselective synthesis of functionalized cyclopent-2-enone-derived carbonylureas and enaminohydroxybarbiturates from alloxans in water

T Abbasi, MB Teimouri, I Yavari, R Bikas, T Lis - Tetrahedron, 2024 - Elsevier
A green one-pot reaction involving cyclic secondary amines, activated alkynes, and alloxan
derivatives in water has been established, offering a cost-effective and selective route to …

[PDF][PDF] 4-Hydroxy-6-methyl-2-pyrone: a versatile synthon in the synthesis of heterocyclic scaffolds via multicomponent reactions

GM Ziarani, R Moradi, M Zandiyeh… - …, 2018 - triggered.stanford.clockss.org
4-Hydroxy-6-methyl-2-pyrone has been utilized in the synthesis of various heterocyclic
compounds. It is a potential 1, 3-dicarbonyl compound with diverse synthetic applications …

Synthesis of spiro oxazolidinedione analogues based on tandem multicyclizations of 1, 3-dimethylalloxan and enaminones in water

T Abbasi, MB Teimouri, I Yavari, R Bikas - Synlett, 2021 - thieme-connect.com
A tandem double-annulation reaction of 1, 3-dimethylalloxan with enaminones, generated in
situ from alkyl amines and alkyl but-2-ynoates or pent-3-yn-2-ones to give functionalized …

Reactions of 1, 4-naphthoquinone and 5-hydroxy-1, 4-naphthoquinone with ninhydrin

LM Gornostaev, OI Fominyh, TI Lavrikova… - Russian Chemical …, 2019 - Springer
Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin Page 1
Russian Chemical Bulletin, International Edition, Vol. 68, No. 1, pp. 86—91, January, 2019 86 …

DFT study on reaction mechanisms of propylamine and dimethyl acetylenedicarboxylate with 1, 3-dimethylalloxan

Y Zhu, Y Li, W Zhang, Q Zhao, M Tang - Computational and Theoretical …, 2013 - Elsevier
In an attempt to explore the mechanism for the multicomponent reaction of propylamine and
dimethyl acetylenedicarboxylate with 1, 3-dimethylalloxan, two reaction mechanisms were …

A practical and convenient method for the synthesis of anesthetic drug thiopental: using thiourea and sodium ethoxide

H Narimani, M Kazemi… - Iranian chemical …, 2014 - icc.journals.pnu.ac.ir
A general, simple, practical and convenient method has been described for the synthesis of
anesthetic drug thiopental using thiourea in the presence of sodium ethoxide. Anesthetic …

An efficient three-component synthesis of new amidinium salts

S Ahadi, M Abaszadeh, HR Khavasi… - Journal of the Iranian …, 2013 - Springer
A simple and efficient method for the synthesis of new amidinate salts containing barbiturate
moiety by a three-component condensation reaction of C–H acids, pyrimidine-tetraone and …