A Recent Update on the Visible Light-promoted Organic Transformations - A Mini-review DOI
Monica Dinodia

Current Organic Synthesis, Год журнала: 2023, Номер 21(8), С. 965 - 975

Опубликована: Авг. 29, 2023

Abstract: Visible light-induced reactions are a rapidly developing and powerful technique to pro-mote organic transformations. They provide green sustainable chemistry have recently re-ceived increasing attention from chemists due their wide application in synthesis. Light energy is eco-friendly, cheap, green, inexhaustible with potential industrial pharmaceutical applications. In this review, the most recent advances visible (2021-till date) been highlighted.

Язык: Английский

Pd-IPent-Catalyzed Defluorinative Annulation of gem-Difluorocyclopropanes with Enamides: Synthesis of Multisubstituted N-H Pyrroles DOI
Wenhao Liu,

Yahui Ma,

Qiuwei Huang

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Фев. 21, 2025

We present a Pd-IPent-catalyzed ring-opening defluorinative annulation reaction of gem-difluorocyclopropanes with enamides, which provides convenient and efficient strategy for the synthesis multisubstituted N-H pyrrole derivatives. This transformation selectively cleaves C1-C3 bond, two C-F bonds, C-N bond in one-pot procedure. Additionally, this protocol allows modification several bioactive molecules.

Язык: Английский

Процитировано

0

Photoredox-Catalyzed gem-Difluoromethylenation of Aliphatic Alcohols with 1,1-Difluoroalkenes to Access α,α-Difluoromethylene Ethers DOI
Xinxin Han, Xin Liu, Christophe Len

и другие.

The Journal of Organic Chemistry, Год журнала: 2023, Номер 88(17), С. 12744 - 12754

Опубликована: Авг. 23, 2023

A switchable synthesis of alcohols and ketones bearing a CF2-OR scaffold using visible-light promotion is described. The method PDI catalysis characterized by its ease operation, broad substrate scopes, the ability to switch between desired products without need for transition metal catalysts. addition or absence base plays key role in controlling major products.

Язык: Английский

Процитировано

6

Selective monodeuteration enabled by bisphosphonium catalyzed ring opening processes DOI Creative Commons

Yuanli Xu,

Wenlong Chen, Ruihua Pu

и другие.

Nature Communications, Год журнала: 2024, Номер 15(1)

Опубликована: Окт. 30, 2024

The selective incorporation of a deuterium atom into small molecules with high selectivity is highly valuable for medical and chemical research. Unfortunately, this remains challenging due to the complete deuteration caused by commonly used hydrogen isotope exchange strategies. We report development photocatalytic monodeuteration protocol utilizing C-C bond as unconventional functional handle. synergistic combination radical-mediated scission transfer processes enables effective constructions benzylic CDH moieties monodeuteration. combinational use bisphosphonium photocatalyst, thiol catalyst, CH

Язык: Английский

Процитировано

2

Probing the Limit of the Number of Saturated Atoms for Achieving Hyperconjugative Aromaticity DOI
Shuwen Chen,

Sajid Imran,

Yu Zhao

и другие.

Inorganic Chemistry, Год журнала: 2024, Номер 63(30), С. 14162 - 14170

Опубликована: Июль 17, 2024

Aromaticity is a fundamental concept in organic chemistry. Hyperconjugative aromaticity, also known as hyperconjugation-induced has evolved from its origin main group substituents to transition metal analogues, establishing itself an important category of aromaticity. Additionally, aromatic compounds comprising two

Язык: Английский

Процитировано

1

Photoredox-Catalyzed Regioselective 1,3-Alkoxypyridylation of gem-Difluorocyclopropanes DOI
Jiaxuan Shen, Meijun Chen, Xiangwei Du

и другие.

Organic Letters, Год журнала: 2024, Номер unknown

Опубликована: Дек. 4, 2024

Difluoromethylene and pyridine cores are very important structural units in medicinal chemistry. Herein, we report the development of photoredox-catalyzed ring-opening 1,3-alkoxypyridylation gem-difluorinated cyclopropanes using 4-cyanopyrines alcohols, employing cyclopropane radical cations as key intermediate. The reaction exhibits high regioselectivity under mild conditions can also be practiced on gram-scale synthesis, telescoped reaction, late-stage functionalization biological molecules.

Язык: Английский

Процитировано

1

Enantioselective Tsuji‐Trost α‐Fluoroallylation of Amino Acid Esters with Gem‐Difluorinated Cyclopropanes DOI
Zhengquan Su,

Binhong Tan,

Hui He

и другие.

Angewandte Chemie, Год журнала: 2024, Номер 136(23)

Опубликована: Фев. 27, 2024

Abstract A novel enantioselective Tsuji–Trost‐type cross coupling reaction between gem ‐difluorinated cyclopropanes and N ‐unprotected amino acid esters enabled by synergistic Pd/Ni/chiral aldehyde catalysis is presented herein. This transformation streamlined the diversity‐oriented synthesis (DOS) of optically active α‐quaternary α‐amino bearing a linear 2‐fluoroallylic motif, which served as an appealing platform for construction other valuable enantioenriched compounds. The key intermediates were confirmed HRMS detection, while DFT calculations revealed that excellent enantioselectivity was attributed to stabilizing non‐covalent interactions Pd(II)‐π‐fluoroallyl species Ni(II)‐Schiff base complex.

Язык: Английский

Процитировано

0

A Recent Update on the Visible Light-promoted Organic Transformations - A Mini-review DOI
Monica Dinodia

Current Organic Synthesis, Год журнала: 2023, Номер 21(8), С. 965 - 975

Опубликована: Авг. 29, 2023

Abstract: Visible light-induced reactions are a rapidly developing and powerful technique to pro-mote organic transformations. They provide green sustainable chemistry have recently re-ceived increasing attention from chemists due their wide application in synthesis. Light energy is eco-friendly, cheap, green, inexhaustible with potential industrial pharmaceutical applications. In this review, the most recent advances visible (2021-till date) been highlighted.

Язык: Английский

Процитировано

0