Recent Advances for the Synthesis of N-Unsubstituted Pyrroles

被引：14

作者：

Efimov, Ilya, V ^{[1
]}

Kulikova, Larisa N. ^{[1
]}

Miftyakhova, Almira R. ^{[1
]}

Matveeva, Maria D. ^{[2
]}

Voskressensky, Leonid G. ^{[1
]}

机构：

[1] RUDN Univ, Peoples Friendship Univ Russia, Res Ctr Mol Design & Synth Innovat Cpds Med, Miklukho Maklaya St 6, Moscow 117198, Russia

[2] Russian Acad Sci, AV Topchiev Inst Petrochem Synth, Leninsky Pr 29, Moscow 119991, Russia

来源：

CHEMISTRYSELECT | 2021年 / 6卷 / 48期

基金：

俄罗斯科学基金会;

关键词：

3+2] annulation; Barton-Zart reaction; cycloaddition reaction; porphyrin; pyrrole; ONE-POT SYNTHESIS; DENSELY FUNCTIONALIZED PYRROLES; DONOR-ACCEPTOR CYCLOPROPANES; HIGHLY SUBSTITUTED PYRROLES; FORMAL 3+2 CYCLOADDITION; SELECTIVE SYNTHESIS; CASCADE REACTION; POLYSUBSTITUTED PYRROLES; MULTICOMPONENT SYNTHESIS; BIOLOGICAL EVALUATION;

D O I：

10.1002/slct.202103486

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Pyrroles are an interesting class of heterocyclic compounds due to their widespread use both in medical chemistry and in the chemistry of new materials. Search and development of new effective methods for the synthesis of the pyrrole ring is an urgent task. Along with this, the systematization of already known synthesis methods is an equally important task. Herein, we focused on the results of the synthesis of NH-pyrroles that have been obtained since 2015.

引用

页码：13740 / 13772

页数：33

共 145 条

[1] Identification of new pyrrolo [2,3-d]pyrimidines as potent VEGFR-2 tyrosine kinase inhibitors: Design, synthesis, biological evaluation and molecular modeling
Adel, Mai
Serya, Rabah A. T.
Lasheen, Deena S.
Abouzid, Khaled A. M.
[J]. BIOORGANIC CHEMISTRY, 2018, 81 : 612 - 629
[2] The role of porphyrin peripheral substituents in determining the reactivities of ferrous nitrosyl species
Amanullah, Sk
Dey, Abhishek
[J]. CHEMICAL SCIENCE, 2020, 11 (23) : 5909 - 5921
[3] [Anonymous], 2015, Chem. - Eur. J.
[4] Sulfenyl Ynamides in Gold Catalysis: Synthesis of Oxo-functionalised 4-aminoimidazolyl Fused Compounds by Intermolecular Annulation Reactions
Arce, Elsa M.
Lamont, Scott G.
Davies, Paul W.
[J]. ADVANCED SYNTHESIS & CATALYSIS, 2020, 362 (12) : 2503 - 2509
[5] Chemoselective cyclization of N-sulfonyl ketimines with ethenesulfonyl fluorides: access to trans-cyclopropanes and fused-dihydropyrroles
Arupula, Sanjeeva Kumar
Gudimella, Santosh K.
Guin, Soumitra
Mobin, Shaikh M.
Samanta, Sampak
[J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (13) : 3451 - 3461
[6] A Critical Review on Advances in the Multicomponent Synthesis of Pyrroles
Azad, Iqbal
Hassan, Firoj
Saquib, Mohammad
Ahmad, Naseem
Khan, Abdul Rahman
Al-Sehemi, Abdillah G.
Nasibullah, Malik
[J]. ORIENTAL JOURNAL OF CHEMISTRY, 2018, 34 (04) : 1670 - 1700
[7] Interaction of 4-oxoalkane-1,1,2,2-tetracarbonitriles with Lawesson's reagent a new approach to the synthesis of 2,2′-disulfanediylbis(1H-pyrroles). The synthesis of photochromic diarylethene with a disulfide bridge
Belikov, Mikhail Yu.
Fedoseev, Sergey V.
Ievlev, Mikhail Yu.
Ershov, Oleg V.
Tafeenko, Victor A.
[J]. RSC ADVANCES, 2015, 5 (80) : 65316 - 65320
[8] Pyrrole: a resourceful small molecule in key medicinal hetero-aromatics
Bhardwaj, Varun
Gumber, Divya
Abbot, Vikrant
Dhiman, Saurabh
Sharma, Poonam
[J]. RSC ADVANCES, 2015, 5 (20): : 15233 - 15266
[9] Pyrroles as Privileged Scaffolds in the Search for New Potential HIV Inhibitors
Bianco, Maria da Conceicao Avelino Dias
Marinho, Debora Inacio Leite Firmino
Hoelz, Lucas Villas Boas
Bastos, Monica Macedo
Boechat, Nubia
[J]. PHARMACEUTICALS, 2021, 14 (09)
[10] Streamlined Synthesis of 6-((1H-1,2,3-Triazol-4-yl)methyl)-1H-pyrrolo [3,4-d]pyridazin-1-one System via Sequential N-Alkylation, CuAAC, and [4+2] Cyclization Reactions
Bonacorso, Helio G.
Magalhaes, Hernane T.
Dal Forno, Gean M.
Libero, Francieli M.
Hoerner, Manfredo
Frizzo, Clarissa P.
Martins, Marcos A. P.
Zanatta, Nilo
[J]. JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2019, 30 (06) : 1189 - 1202

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