ChemInform Abstract: Synthesis of Multisubstituted 1H‐Pyrrole: Selenium‐Catalyzed Reaction of γ‐Nitro Substituted Carbonyl Compounds and Carbon Monoxide. DOI

Rui Umeda,

Tsukasa Mashino,

Yutaka Nishiyama

и другие.

ChemInform, Год журнала: 2014, Номер 45(47)

Опубликована: Ноя. 6, 2014

Abstract γ‐Nitro‐substituted carbonyl compounds undergo a selenium catalyzed reductive cyclization with CO as reducing agent to yield multi‐ fully‐substituted pyrroles (II) and (IV).

Язык: Английский

Selenium reagents as catalysts DOI
Fateh V. Singh, Thomas Wirth

Catalysis Science & Technology, Год журнала: 2019, Номер 9(5), С. 1073 - 1091

Опубликована: Янв. 1, 2019

Organoselenium chemistry has become an important tool in synthetic and medicinal chemistry.

Язык: Английский

Процитировано

171

Microwave-Promoted Tin-Free Iminyl Radical Cyclization with TEMPO Trapping: A Practical Synthesis of 2-Acylpyrroles DOI
Yu Cai, Ankur Jalan,

Aaron R. Kubosumi

и другие.

Organic Letters, Год журнала: 2015, Номер 17(3), С. 488 - 491

Опубликована: Янв. 16, 2015

Microwave-promoted iminyl radical cyclizations can be terminated by trapping with TEMPO, affording functionalized adducts. The use of alkynes as acceptors delivers a range 2-acylpyrroles in good yields. Toxic and hazardous reagents, which are frequently employed reactions, not required. O-phenyl oxime ether substrates constructed single step from readily available ketones.

Язык: Английский

Процитировано

73

Recent advances in organic synthesis applying elemental selenium DOI
Tao Guo, Zhonghui Li,

Lei Bi

и другие.

Tetrahedron, Год журнала: 2022, Номер 112, С. 132752 - 132752

Опубликована: Март 31, 2022

Язык: Английский

Процитировано

33

Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source DOI

Pavel N. Kolesnikov,

Niyaz Z. Yagafarov,

Dmitry L. Usanov

и другие.

Organic Letters, Год журнала: 2014, Номер 17(2), С. 173 - 175

Опубликована: Дек. 31, 2014

A ruthenium-catalyzed reductive amination without an external hydrogen source has been developed using carbon monoxide as the reductant and ruthenium(III) chloride (0.008–2 mol %) catalyst. The method was applied to synthesis of antianxiety agent ladasten.

Язык: Английский

Процитировано

55

Recent Advances in Organoselenium Catalysis DOI
G. Santosh,

Samata E. Shetgaonkar,

Fateh V. Singh

и другие.

Current Organic Synthesis, Год журнала: 2022, Номер 19(3), С. 393 - 413

Опубликована: Фев. 11, 2022

Abstract: : Organoselenium chemistry has developed as an important tool in the field of synthetic and medicinal chemistry. Various organoselenium reagents have been used successfully to achieve different organic transformations such selenocyclizations, oxyselenenylations selenoxide eliminations etc. Additionally, potential is not limited their use stoichiometric but they organocatalyst number transformations. inorganic oxidants identified terminal regenerate active catalytic specie. In this review article, recent progress catalysis being highlighted along with asymmetric variants.

Язык: Английский

Процитировано

23

Recent advances in chemistry of β-cyano ketones DOI
Nicolai A. Aksenov, Дмитрий А. Аксенов,

A. E. Kurlikov

и другие.

Russian Chemical Bulletin, Год журнала: 2025, Номер 74(2), С. 305 - 327

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Recent Advances in the Synthesis of Pyrroles DOI

Sarosh Iqbal,

Hina Rasheed,

Rabiya Javed Awan

и другие.

Current Organic Chemistry, Год журнала: 2020, Номер 24(11), С. 1196 - 1229

Опубликована: Май 28, 2020

Pyrroles are the most prevalent heterocyclic compounds, which present as basic cores in many natural products, such vitamin B12, bile pigments like bilirubin and biliverdin, porphyrins of heme, chlorophyll, chlorins, bacteriochlorins, porphyrinogens. The biological activities compounds having pyrrole analogs include antimicrobial (antibacterial, antifungal), anti-cancer (anti-cytotoxic, antimitotic), anti-tumor, anti-hyperlipidemic, anti-depressant, anti-inflammatory, antihyperglycemic, antiproliferative, anti-HIV anti-viral activities. Accordingly, significant attention has been paid to develop competent methods for synthesis pyrroles with improved yields short times. This review gives an overview different using easily available precursors following routes. Synthesis monosubstituted 2,5-dimethoxyfuran dialkylacetylene dicarboxylate β-ketoester 1,2-dicarbonyl 1,3-dicarbonyl 1,3-dicarbonyl, amine, nitro aldehyde group 1,4-dicarbonyl compound amines enones moieties acetylene

Язык: Английский

Процитировано

24

Recent Advances in Selenium‐Mediated Redox Functional Group Interconversions DOI Creative Commons
Antonella Capperucci, Damiano Tanini

The Chemical Record, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 22, 2024

Abstract The conversion of a functional group into another represents the core organic synthesis. Within arena interconversions, oxidative and reductive transformations occupy privileged position development new sustainable, selective, general methodologies continue to attract significant interest. Owing versatility their chemistry, selenium compounds offer opportunities achieve both oxidation reduction wide range groups. Additionally, possibility generate in situ active oxidant or reducing species from suitable inert precursors enables catalytic processes. In this review, recent advances selenium‐mediated with particular emphasis on cutting‐edge researches bringing about insights comprehension mechanistic aspects, will be discussed.

Язык: Английский

Процитировано

2

The squaramide-catalyzed asymmetric Michael/cyclization tandem reaction for the synthesis of chiral trifluoromethylated hydroxyimino tetrahydrobenzofuranones DOI
Wei Liu,

Xiaoyan Lai,

Gao‐Feng Zha

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2016, Номер 14(14), С. 3603 - 3607

Опубликована: Янв. 1, 2016

This paper presents efficient access to chiral hydroxyimino tetrahydrobenzofuranones featuring a trifluoromethyl group at an all-carbon quaternary stereocenter.

Язык: Английский

Процитировано

15

Selenium-Assisted Reduction of Sulfur Dioxide by Carbon Monoxide in the Liquid Phase DOI

Bentao Yang,

Liyuan Chai, Fangfang Zhu

и другие.

Industrial & Engineering Chemistry Research, Год журнала: 2017, Номер 56(8), С. 1895 - 1902

Опубликована: Фев. 3, 2017

Regenerable flue gas desulfurization (FGD) is highly attractive because of the transformation sulfur dioxide (SO2) to high-value products. In this study, selenium-assisted SO2 reduction by carbon monoxide (CO) in liquid phase [dimethylformamide (DMF) + water (H2O) mixture] proposed and applied FGD process. This process realizes recycle elemental product under room temperature. Moreover, results show that both selenium catalyst DMF solvent have good stability can be well recycled, implying economically feasible. Furthermore, mechanism CO DMF/H2O investigated. Results dissolves solution forms Sen2– species, which are active intermediates promote formation product.

Язык: Английский

Процитировано

10