Remote Selective C−H Halogenation of Arylphosphine Oxides with Ferric Halides DOI
Hong Yu,

Xiuhua Lin,

Guang Xu

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2023, Номер 365(18), С. 3101 - 3106

Опубликована: Авг. 16, 2023

Abstract We developed the remote selective C−H bromination for synthesis of C4′‐brominated biarylphosphine oxides using FeBr 3 as a brominating reagent. C3′‐Brominated products were obtained in reactions with substrates bearing 2,4,6‐triisopropyl substituent on bottom ring. Moreover, direct access to C5‐chlorinated peri ‐substituted(1‐naphthalenyl)phosphines is FeCl chlorinating These halogenated compounds can be utilized cross‐coupling construct functionalized phosphine oxides.

Язык: Английский

Copper-Catalyzed C–C Cross-Couplings of Tertiary Alkyl Halides with Anilines Enabled by Cyclopropenimine-Based Ligands DOI

Serim Choi,

Yongseok Choi,

Yong‐Jae Kim

и другие.

Journal of the American Chemical Society, Год журнала: 2023, Номер unknown

Опубликована: Ноя. 6, 2023

Catalytic cross-couplings of tertiary alkyl electrophiles with carbon nucleophiles offer a powerful platform for constructing quaternary centers, which are prevalent in bioactive molecules. However, these reactions remain underdeveloped primarily because steric challenges that impede efficient bond formation. Herein, we describe the copper-catalyzed synthesis such centers through C(sp3)-C(sp2) bond-forming reaction between halides and arene rings aniline derivatives, enabled by strategic implementation bidentate bis(cyclopropenimine) ligands. The copper catalyst bound two imino-nitrogen atoms ligands, have never been employed metal catalysis previously, is highly effective rapidly activating to generate radicals, allowing them react aryl under mild conditions remarkably short times (1-2 h). Various bearing carbonyl functional groups can be coupled secondary or primary anilines, furnishing range good yields. Several mechanistic observations support generation copper(II) species radicals as result elucidate steps proposed catalytic cycle.

Язык: Английский

Процитировано

1

Sterically demanding Csp2(ortho-substitution)–Csp3(tertiary) bond formation via carboxylate-directed Mizoroki-Heck reaction under extra-ligand-free conditions DOI Creative Commons
Wei Zeng,

A. CHEN,

Ming‐Jie Yan

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2023, Номер 22(1), С. 80 - 84

Опубликована: Ноя. 22, 2023

Construction of the sterically demanding Csp2(oS)-Csp3(T) bond was achieved by carrying out Pd-catalyzed carboxylate-directed Mizoroki-Heck reaction under extra-ligand-free aqueous conditions. The cooperative role presence water with absence phosphine ligand proposed to accelerate migratory insertion process considerably, delivering a broad substrate scope.

Язык: Английский

Процитировано

1

Macrocyclic Sulfur Ligand Stabilized Trans‐Palladium Dichloride Complex: Syntheses, Structure, Chlorine Rotation, and Application in α‐Olefination of Nitriles by Primary Alcohols DOI
Sunil Kumar, Ashutosh Sharma, Suman Mahala

и другие.

Chemistry - An Asian Journal, Год журнала: 2023, Номер 19(4)

Опубликована: Дек. 20, 2023

Herein, we have reported the synthesis of a macrocyclic organosulfur ligand (L1) having seventeen-membered ring. Subsequently, corresponding trans-palladium complex (C1) bulky was synthesized by reacting it with PdCl

Язык: Английский

Процитировано

1

Remote Selective C−H Halogenation of Arylphosphine Oxides with Ferric Halides DOI
Hong Yu,

Xiuhua Lin,

Guang Xu

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2023, Номер 365(18), С. 3101 - 3106

Опубликована: Авг. 16, 2023

Abstract We developed the remote selective C−H bromination for synthesis of C4′‐brominated biarylphosphine oxides using FeBr 3 as a brominating reagent. C3′‐Brominated products were obtained in reactions with substrates bearing 2,4,6‐triisopropyl substituent on bottom ring. Moreover, direct access to C5‐chlorinated peri ‐substituted(1‐naphthalenyl)phosphines is FeCl chlorinating These halogenated compounds can be utilized cross‐coupling construct functionalized phosphine oxides.

Язык: Английский

Процитировано

0