Tetrabutylammonium decatungstate (TBADT), a compelling and trailblazing catalyst for visible-light-induced organic photocatalysis DOI
Bor‐Cherng Hong, Ranadheer Reddy Indurmuddam

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(19), С. 3799 - 3842

Опубликована: Янв. 1, 2024

Tetrabutylammonium decatungstate (TBADT) has recently emerged as an intriguing photocatalyst under visible-light or near-visible-light irradiation in a wide range of organic reactions that were previously not conceivable. Given its ability to absorb visible light and excellent effectiveness activating unactivated chemical bonds, it is promising addition traditional photocatalysts. This review covers some the contemporary developments photocatalysis enabled by TBADT catalyst 2023, with contents organized reaction type.

Язык: Английский

Asymmetric alkyl-alkyl cross-coupling enabled by earth-abundant metal-catalyzed hydroalkylations of olefins DOI Creative Commons
Pengfei Yang, Wei Shu

Chem Catalysis, Год журнала: 2023, Номер 3(4), С. 100508 - 100508

Опубликована: Янв. 30, 2023

Язык: Английский

Процитировано

28

Designed Iron Catalysts for Allylic C−H Functionalization of Propylene and Simple Olefins DOI

Ruihan Wang,

Yidong Wang, Ruiqi Ding

и другие.

Angewandte Chemie International Edition, Год журнала: 2023, Номер 62(10)

Опубликована: Янв. 9, 2023

Abstract Propylene gas is produced worldwide by steam cracking on million‐metric‐ton scale per year. It serves as a valuable starting material for π‐bond functionalization but rarely applied in transition metal‐catalyzed allylic C−H fine chemical synthesis. Herein, we report that newly‐developed cationic cyclopentadienyliron dicarbonyl complex allows the conversion of propylene to its C−C bond coupling products under catalytic conditions. This approach was also found applicable simple α‐olefins with distinctive branched selectivity. Experimental and computational mechanistic studies supported deprotonation metal‐coordinated alkene turnover‐limiting step led insights into multifaceted roles newly designed ligand promoting enhanced reactivity stereoselectivity.

Язык: Английский

Процитировано

23

Catalytic Enantioselective Primary C–H Borylation for Acyclic All-Carbon Quaternary Stereocenters DOI

Yuhuan Yang,

Jingyao Chen,

Yongjia Shi

и другие.

Journal of the American Chemical Society, Год журнала: 2024, Номер 146(2), С. 1635 - 1643

Опубликована: Янв. 5, 2024

Creating a perfect catalyst to operate enzyme-like chiral recognition has been long-sought aim. A challenging example in this context is constructing acyclic all-carbon quaternary stereogenic centers by transition metal-catalyzed enantioselective C–H activation. We now report highly iridium-catalyzed primary borylation of α-all-carbon substituted 2,2-dimethyl amides enabled tailor-made bidentate boryl ligand (CBL). The success the current transformation attributed CBL/iridium catalyst, which confined pocket. This protocol provides diverse array stereocenters with excellent enantiocontrol and distinct structural features. Computational study reveals that steric hindrance CBL could regulate type dominant orbital interaction between substrate, crucial conferring high induction.

Язык: Английский

Процитировано

13

Recent advances in Rh(i)-catalyzed enantioselective C–H functionalization DOI Creative Commons
Yue Zhang, Jing‐Jing Zhang, Lujun Lou

и другие.

Chemical Society Reviews, Год журнала: 2024, Номер 53(7), С. 3457 - 3484

Опубликована: Янв. 1, 2024

Chiral carbon-carbon (C-C) and carbon-heteroatom (C-X) bonds are pervasive very essential in natural products, bioactive molecules, functional materials, their catalytic construction has emerged as one of the hottest research fields synthetic organic chemistry. The last decade witnessed vigorous progress Rh(I)-catalyzed asymmetric C-H functionalization a complement to Rh(II) Rh(III) catalysis. This review aims provide most comprehensive up-to-date summary covering recent advances activation for functionalization. In addition development diverse reactions, chiral ligand design mechanistic investigation (inner-sphere mechanism, outer-sphere 1,4-Rh migration) will also be highlighted.

Язык: Английский

Процитировано

13

Tetrabutylammonium decatungstate (TBADT), a compelling and trailblazing catalyst for visible-light-induced organic photocatalysis DOI
Bor‐Cherng Hong, Ranadheer Reddy Indurmuddam

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(19), С. 3799 - 3842

Опубликована: Янв. 1, 2024

Tetrabutylammonium decatungstate (TBADT) has recently emerged as an intriguing photocatalyst under visible-light or near-visible-light irradiation in a wide range of organic reactions that were previously not conceivable. Given its ability to absorb visible light and excellent effectiveness activating unactivated chemical bonds, it is promising addition traditional photocatalysts. This review covers some the contemporary developments photocatalysis enabled by TBADT catalyst 2023, with contents organized reaction type.

Язык: Английский

Процитировано

12