Iron-Catalyzed C–C Bond Cleavage of Oximes for Direct Coupling of Benzothiazole in Water DOI

Wuxin Zhou,

Yang Long, Haifeng Xiang

et al.

The Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 88(7), P. 4875 - 4879

Published: March 29, 2023

An Fe-catalyzed coupling reaction between oxime ester and benzothiazole is described, which involves C-C bond cleavage of via a single-electron transfer process. This iron catalytic system performed in water under mild conditions offers streamlined strategy to the construction alkyl nitrile substituted derivatives. Application this for synthesis some key important compounds including 4-heterocyclic-3-arylbutanoic acid also reported.

Language: Английский

Nickel‐Catalyzed Regio‐ and Stereoselective Defluorinative Arylation of gem‐Difluorinated Cyclopropanes DOI Open Access
Shutao Qi,

Yunkai Hua,

Liangkai Pan

et al.

Chinese Journal of Chemistry, Journal Year: 2023, Volume and Issue: 42(8), P. 823 - 828

Published: Dec. 8, 2023

Comprehensive Summary Herein, we report nickel‐catalyzed cross‐coupling of gem ‐difluorinated cyclopropanes with boronic acids, providing the corresponding arylated 2‐fluoroallylic scaffolds. This approach used commercially available phosphine ligand Xantphos to obtain monofluorinated alkenes high regioselectivity and Z ‐stereoselectivity. Mechanistic studies proposed a Ni(II)‐fluoroallyl pathway excluded radical pathway. Meanwhile, DFT study reductive elimination clarified origin linear selectivity.

Language: Английский

Citations

8

Pd-IHept-Catalyzed Ring-Opening of gem-Difluorocyclopropanes with Malonates Via Selective C–C Bond Cleavage: Synthesis of Monofluoroalkenes DOI
Yuxuan Yan, Huijun Qian, Leiyang Lv

et al.

The Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 89(22), P. 16253 - 16261

Published: Sept. 22, 2023

Monofluoroalkene scaffolds are frequently found in various functional molecules. Herein, we report a Pd-IHept-catalyzed (NHC = N-heterocyclic carbene) defluorinative functionalization approach for the synthesis of monofluoroalkenes from

Language: Английский

Citations

7

Carbofluorination of Alkenes with gem-Difluorinated Cyclopropanes as Bifunctional Reagents Enabled by Well-Define Rhodium Catalysts DOI Creative Commons
Yaxin Zeng, Zhong‐Tao Jiang,

Yulei Zhu

et al.

Published: Aug. 21, 2023

Herein, we report a Rh-catalyzed carbofluorination of alkenes using gem-difluorinated cyclopropanes as bifunctional reagents. The developed method tolerates wide range alkenes, providing access to secondary, tertiary fluorides and gem-difluorides with 100% atom-economy under mild conditions. resulting can be further transformed yield C−C, C−N, C−O bifunctionalization products. Cationic dicarbonyl rhodium tetrafluoroborate has been identified the only highly efficient catalyst in this reaction. Preliminary mechanistic studies reveal that addition fluorine atom is mediated by ion, which acts anion shuttle.

Language: Английский

Citations

6

Pd-catalyzed access to mono- and di-fluoroallylic amines from primary anilines DOI Creative Commons

Xingben Wang,

Frédéric W. Patureau

Chemical Communications, Journal Year: 2022, Volume and Issue: 59(4), P. 486 - 489

Published: Dec. 16, 2022

The Pd-catalyzed highly selective synthesis of mono- and di-2-fluoroallylic amines from gem-difluorocyclopropanes ubiquitous unprotected primary anilines is herein described. Initial kinetic investigations suggest a first order in the gem-difluorocyclopropane substrate, as well circa zeroth aniline coupling partner. newly produced fluoroallylic motifs should find important applications synthetic medicinal chemistry stimulate further development methods based on strained cyclic building blocks.

Language: Английский

Citations

9

Iron-Catalyzed C–C Bond Cleavage of Oximes for Direct Coupling of Benzothiazole in Water DOI

Wuxin Zhou,

Yang Long, Haifeng Xiang

et al.

The Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 88(7), P. 4875 - 4879

Published: March 29, 2023

An Fe-catalyzed coupling reaction between oxime ester and benzothiazole is described, which involves C-C bond cleavage of via a single-electron transfer process. This iron catalytic system performed in water under mild conditions offers streamlined strategy to the construction alkyl nitrile substituted derivatives. Application this for synthesis some key important compounds including 4-heterocyclic-3-arylbutanoic acid also reported.

Language: Английский

Citations

4