Calcium carbide: Highly potent solid reagent for the construction of heterocycles

Tetrahedron, Год журнала: 2023, Номер 149, С. 133720 - 133720

Опубликована: Ноя. 1, 2023

Язык: Английский

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Construction of 3-Methyl-2-Substituted Benzo[b]furans and 3-Methyl-2-Substituted Benzo[b]thiophenes Using Solid Calcium Carbide as a Substitute for Gaseous Acetylene

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(10), С. 7182 - 7186

Опубликована: Май 2, 2024

A concise method for the facile construction of 3-methyl-2-substituted benzo[b]furans and benzo[b]thiophenes using low-cost, abundant, easy-to-use solid calcium carbide instead flammable explosive gaseous acetylene as an original alkyne source, o-bromophenyl ethers or thioethers substrates through intramolecular carbanion-yne cyclization in a 5-exo-dig manner, subsequent double-bond isomerization is described. The simultaneous formation two C–C bonds realized one-step route. wide substrate scope, high yield, simple workup manipulations are also merits this method. synthetic strategy can be suitable gram scale.

Язык: Английский

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Construction of Pyrazolo[1,5-a]pyrimidines and Pyrimido[1,2-b]indazoles with Calcium Carbide as an Alkyne Source

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(28), С. 5822 - 5826

Опубликована: Янв. 1, 2024

One-step construction of both 5-arylpyrazolo[1,5- a ]pyrimidines and 2-arylpyrimido[1,2- b ]indazoles using inexpensive, abundant easy-to-handle calcium carbide as solid alkyne source is depicted.

Язык: Английский

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Highly Stereoselective Synthesis of 2-Acyl-3-sulfonamidobut-2-enoates Using Solid Calcium Carbide as a Substitute for Gaseous Acetylene

Organic Letters, Год журнала: 2024, Номер 26(29), С. 6269 - 6273

Опубликована: Июль 17, 2024

Multifunctional group compounds, 2-acyl-3-sulfonamidobut-2-enoates, are efficiently constructed using solid calcium carbide as an alkyne source through the simultaneous formation of two bonds in one step. The salient features this protocol use inexpensive, abundant, and easy-to-use a substitute for flammable explosive gaseous acetylene, low-cost catalyst, mild conditions, wide substrate scope, high stereoselectivity, satisfactory yield, simple manipulation. This method can also be extended to gram scale.

Язык: Английский

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One-step construction of indolo[2,1- a ]isoquinolines using solid calcium carbide as an alternative to gaseous acetylene

Synthetic Communications, Год журнала: 2024, Номер 54(14), С. 1209 - 1219

Опубликована: Июль 17, 2024

Язык: Английский

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The Use of Calcium Carbide for Cyclopentenone Ring Construction

Russian Journal of General Chemistry, Год журнала: 2024, Номер 94(1), С. 45 - 48

Опубликована: Янв. 1, 2024

Язык: Английский

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Three-component one-pot construction of 2-aryl-3-benzylbenzo[4,5]imidazo[1,2- a ]pyrimidines using solid calcium carbide as an alkyne source

Synthetic Communications, Год журнала: 2025, Номер unknown, С. 1 - 11

Опубликована: Фев. 16, 2025

Язык: Английский

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1,2-Dichloroethane as a Gaseous Acetylene Source for the Rapid Assembly of Isoquinolino[1,2-b]quinazolinone Scaffolds

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 9, 2025

Reported herein is a novel ruthenium(II)-catalyzed [4 + 2] annulation of quinazolinones with 1,2-dichloroethane (DCE), resulting in myriad isoquinolino[1,2-b]quinazolinone scaffolds. In this protocol, DCE serves not only as solvent but also an acetylene source. The fused undergo versatile transformations and provide rapid convenient way to access several important bioactive molecule analogues such Rutecarpine, Euxylophoricine B E. potential reaction pathway was elucidated through detailed mechanistic studies Density Functional Theory (DFT) calculations.

Язык: Английский

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Recent progress in the catalytic transformation of acetylene

Chemical Society Reviews, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Acetylene, a traditional industrial raw material, has garnered increasing attention in modern organic synthesis over the past two decades.

Язык: Английский

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One‐Pot Three‐Component Construction of (Z)‐3‐Benzylidene‐2‐(quinolin‐8‐yl)isoindolin‐1‐ones Through C(sp²)−H Bond Activation Using Calcium Carbide as a Solid Alkyne Source

ChemistrySelect, Год журнала: 2024, Номер 9(33)

Опубликована: Сен. 4, 2024

Abstract A simple method for the synthesis of (Z)‐3‐benzylidene‐2‐(quinolin‐8‐yl)isoindolin‐1‐ones through C(sp 2 )−H bond activation, Sonogashira cross‐coupling and annulation tandem reactions using calcium carbide as a solid alkyne source, benzamides starting materials is described. The inexpensive easy‐to‐handle first employed coupling partner in non‐activated activation. one‐pot three‐component proceed efficiently with broad range substrates good tolerance diversity functional groups. reaction routes can also be scaled up to gram scale.

Язык: Английский

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