Aryne Aminohalogenation Using Protic Amines Enabled by Halogen Transfer DOI
Joshua Gavin,

Lars Anderson,

Courtney C. Roberts

и другие.

Organic Letters, Год журнала: 2024, Номер 26(36), С. 7530 - 7534

Опубликована: Авг. 28, 2024

Methods for aryne difunctionalization have been the focus of recent research, but one limitation is use nucleophiles with proton sources. Herein, we demonstrate halogen transfer reagents to enable protic amines in aminohalogenation difunctionalizations up 86% yield. This method uses and arynes a variety N-heterocyclic scaffolds. Through derivatizations, synthetic utility these products demonstrated.

Язык: Английский

Thioxanthone Synthesis from Thioureas through Double Aryne Insertion into a Carbon-Sulfur Double Bond DOI Creative Commons

Mikio Kawada,

Shinya Tabata,

Yusuke Hoshi

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Янв. 9, 2025

Thioxanthone synthesis from o-silylaryl triflates and thioureas is disclosed. Double aryne insertion into the C═S double bond of subsequent hydrolysis realized facile preparation thioxanthones. A simple reaction procedure good accessibility allowed us to synthesize a wide range highly functionalized

Язык: Английский

Процитировано

0

Fe3O4@SiO2-Diol/AQ-Pd(0) nanocomposite catalyzed ecofriendly synthesis of thioesters via three-component thiocarbonylation-coupling reactions DOI

Fadhel F. Sead,

Vicky Jain,

R Roopashree

и другие.

Journal of Organometallic Chemistry, Год журнала: 2025, Номер unknown, С. 123654 - 123654

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

Transition metal-free synthesis of polyfluoroaryl sulfides via S-transfer reaction DOI

Yuhua Wang,

Mengqin Liu,

Heye Zhou

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(19), С. 5558 - 5563

Опубликована: Янв. 1, 2024

A simple, general, thiol- and metal-free method for the synthesis of symmetrical unsymmetrical polyfluorodiaryl sulfides polyfluoroaryl-alkyl sulfides.

Язык: Английский

Процитировано

2

Aryne Aminohalogenation Using Protic Amines Enabled by Halogen Transfer DOI
Joshua Gavin,

Lars Anderson,

Courtney C. Roberts

и другие.

Organic Letters, Год журнала: 2024, Номер 26(36), С. 7530 - 7534

Опубликована: Авг. 28, 2024

Methods for aryne difunctionalization have been the focus of recent research, but one limitation is use nucleophiles with proton sources. Herein, we demonstrate halogen transfer reagents to enable protic amines in aminohalogenation difunctionalizations up 86% yield. This method uses and arynes a variety N-heterocyclic scaffolds. Through derivatizations, synthetic utility these products demonstrated.

Язык: Английский

Процитировано

1