Open Access
Open access

Dimroth-type N/S-interchange ofN-aminothioglycolurils in the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolones

Vinogradova E.E., Gazieva G.A., Izmest'ev A.N., Karnoukhova V.A., Kravchenko A.N.
Тип документаJournal Article
Дата публикации2021-08-14
Название журналаRSC Advances
ИздательThe Royal Society of Chemistry
КвартильQ1
ISSN20462069
  • General Chemistry
  • General Chemical Engineering
Краткое описание

An original method for the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolone derivatives has been developed based on an acid-induced Dimroth-type N/S-interchange of N-aminothioglycolurils formed in situ into 2-hydrazonoimidazo[4,5-d]thiazolones.

Пристатейные ссылки: 30
Цитируется в публикациях: 0
The Dimroth Rearrangement in the Synthesis of Condensed Pyrimidines – Structural Analogs of Antiviral Compounds
Mamedov V.А., Zhukova N.А., Kadyrova M.S.
Q3 Chemistry of Heterocyclic Compounds 2021 цитирований: 2
An Efficient Procedure of Synthesis Acyclic C-Glycosides of Thiazolo [4, 5-b]Pyrazine and Imidazo[4,5-d]Thiazole with Expected Anti-Cancer Activities
Ghoneim A.A., Ali Hassan A.G.
Q3 Polycyclic Aromatic Compounds 2020 цитирований: 1
Dimroth´s Rearrangement as a Synthetic Strategy Towards New Heterocyclic Compounds
Ferreira V.F., de B. da Silva T., Pauli F.P., Ferreira P.G., da S. M. Forezi L., de S. Lima C.G., de C. da Silva F.
Q2 Current Organic Chemistry 2020 цитирований: 3
ANALYSIS OF XRD STRUCTURAL PARAMETERS OF GLYCOLURIL AND ITS DERIVATIVES
Panshina S.Y., Ponomarenko O.V., Bakibaev A.A., Malkov V.S.
Q4 Journal of Structural Chemistry 2020 цитирований: 3
Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems
Makhova N.N., Belen’kii L.I., Gazieva G.A., Dalinger I.L., Konstantinova L.S., Kuznetsov V.V., Kravchenko A.N., Krayushkin M.M., Rakitin O.A., Starosotnikov A.M., Fershtat L.L., Shevelev S.A., Shirinian V.Z., Yarovenko V.N.
Q1 Russian Chemical Reviews 2020 цитирований: 29
The literature of heterocyclic chemistry, part XVIII, 2018
Belen’kii L.I., Gazieva G.A., Evdokimenkova Y.B., Soboleva N.O.
Q1 Advances in Heterocyclic Chemistry 2020 цитирований: 2
Trifluoromethyl–containing 1,2,4-triazines. Synthesis on the base of perfluorobiacetyl and reactions with thiosemicarbazide and thiourea
Saloutina L.V., Zapevalov A.Y., Kodess M.I., Slepukhin P.A., Ganebnykh I.N., Saloutin V.I., Chupakhin O.N.
Q2 Journal of Fluorine Chemistry 2019 цитирований: 5
Role of sulphur-heterocycles in medicinal chemistry: An update
Pathania S., Narang R.K., Rawal R.K.
Q1 European Journal of Medicinal Chemistry 2019 цитирований: 49
Biotin in metabolism, gene expression, and human disease
León‐Del‐Río A.
Q1 Journal of Inherited Metabolic Disease 2019 цитирований: 23
Synthesis of trifluoromethyl – containing oxo(thioxo)imidazothiazolones and thioglycolurils based on perfluorobiacetyl
Saloutina L.V., Zapevalov A.Y., Kodess M.I., Ganebnykh I.N., Saloutin V.I., Chupakhin O.N.
Q2 Journal of Fluorine Chemistry 2018 цитирований: 3
Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils
Gazieva G.A., Nechaeva T.V., Kostikova N.N., Sigay N.V., Serkov S.A., Popkov S.V.
Q3 Russian Chemical Bulletin 2018 цитирований: 9
Dimroth Rearrangement-Old but not Outdated
Krajczyk A., Boryski J.
Q2 Current Organic Chemistry 2017 цитирований: 12
Natural Products with Heteroatom-Rich Ring Systems
Davison E.K., Sperry J.
Q1 Journal of Natural Products 2017 цитирований: 34
Synthesis, biological evaluation and quantitative structure-active relationships of 1,3-thiazolidin-4-one derivatives. A promising chemical scaffold endowed with high antifungal potency and low cytotoxicity
Carradori S., Bizzarri B., D'Ascenzio M., De Monte C., Grande R., Rivanera D., Zicari A., Mari E., Sabatino M., Patsilinakos A., Ragno R., Secci D.
Q1 European Journal of Medicinal Chemistry 2017 цитирований: 14
A Synopsis of the Properties and Applications of Heteroaromatic Rings in Medicinal Chemistry
Meanwell N.A.
Q1 Advances in Heterocyclic Chemistry 2017 цитирований: 15
Метрики
Поделиться
Цитировать
ГОСТ |
Цитировать
1. Vinogradova E.E. и др. Dimroth-type N/S-interchange of N-aminothioglycolurils in the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolones // RSC Advances. 2021. Т. 11. № 45. С. 28395–28400.
RIS |
Цитировать

TY - JOUR

DO - 10.1039/d1ra05568b

UR - http://dx.doi.org/10.1039/d1ra05568b

TI - Dimroth-type N/S-interchange of N-aminothioglycolurils in the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolones

T2 - RSC Advances

AU - Vinogradova, Ekaterina E.

AU - Gazieva, Galina A.

AU - Izmest'ev, Alexei N.

AU - Karnoukhova, Valentina A.

AU - Kravchenko, Angelina N.

PY - 2021

PB - Royal Society of Chemistry (RSC)

SP - 28395-28400

IS - 45

VL - 11

SN - 2046-2069

ER -

BibTex |
Цитировать

@article{2021,

doi = {10.1039/d1ra05568b},

url = {https://doi.org/10.1039%2Fd1ra05568b},

year = 2021,

publisher = {Royal Society of Chemistry ({RSC})},

volume = {11},

number = {45},

pages = {28395--28400},

author = {Ekaterina E. Vinogradova and Galina A. Gazieva and Alexei N. Izmest{\textquotesingle}ev and Valentina A. Karnoukhova and Angelina N. Kravchenko},

title = {Dimroth-type N/S-interchange of N-aminothioglycolurils in the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolones}

}

MLA
Цитировать
Vinogradova, Ekaterina E. et al. “Dimroth-Type N/S-Interchange of N-Aminothioglycolurils in the Synthesis of 2-Hydrazonoimidazo[4,5-D]thiazolones.” RSC Advances 11.45 (2021): 28395–28400. Crossref. Web.