Nickel‐Catalysis Enabling α‐Alkylation of Ketones by Secondary Alcohols DOI

Amreen K. Bains,

Ayanangshu Biswas, Abhishek Kundu

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2022, Номер 364(16), С. 2815 - 2821

Опубликована: Июль 11, 2022

Abstract The α‐alkylation of ketones utilizing a secondary alcohol has been accomplished by an isolable, bench‐stable, inexpensive nickel catalyst affording high yields β,β‐disubstituted products. This report contributes in the pool few scarce examples base metal discovered for this purpose. substrate scope can span wide range including aliphatic, alicyclic, and cyclic alcohols. Functionalization cholesterol molecule is also possible following methodology. interconvert between azo hydrazo form reversible fashion to enable chemical transformation. magnified image

Язык: Английский

Recent advances in C/N-alkylation with alcohols through hydride transfer strategies DOI
Mahdi Jafarzadeh,

Seyed Hasan Sobhani,

Karol Gajewski

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2022, Номер 20(39), С. 7713 - 7745

Опубликована: Янв. 1, 2022

Recent advances in C/N alkylation using alcohols as alkylating reagents via hydrogen-shuttle methodologies: Borrowing Hydrogen, Acceptorless Dehydrogenative Coupling, and Base-mediated Hydride Transfer.

Язык: Английский

Процитировано

20

A strategic approach for Csp3–H functionalization of 9H-fluorene: an acceptorless dehydrogenation and borrowing hydrogen approach DOI
Rahul Sharma, Avijit Mondal,

Arup Samanta

и другие.

Catalysis Science & Technology, Год журнала: 2023, Номер 13(3), С. 611 - 617

Опубликована: Янв. 1, 2023

Herein, we described the selective synthesis of both alkylated and alkenylated fluorenes using a single SNS ligand derived nickel complex.

Язык: Английский

Процитировано

12

Bis-Triazolylidenes of Manganese and Rhenium and Their Catalytic Application in N-Alkylation of Amines with Alcohols DOI Creative Commons
Sofia Friães, Clara S. B. Gomes, Beatriz Royo

и другие.

Organometallics, Год журнала: 2023, Номер 42(14), С. 1803 - 1809

Опубликована: Апрель 11, 2023

A new family of air-stable Mn and Re complexes bearing bidentate bis(1,2,3-triazol-5-ylidene) ligands with the general formula [M(bis-triazolylidene)(CO)3X] (M = or Re; X Cl Br), containing a methylene linker direct link between two triazolylidene ligands, is presented. All have been applied as catalysts for N-alkylation anilines benzylic alcohols. The complex bis-triazolylidene bridge fragments was shown to be highly efficient catalyst, affording corresponding amine in 92% yield presence low base loading (t-BuOK, 0.1 equiv). Comparison imidazolium- triazolium-derived N-heterocyclic carbene showed that triazolylidenes displayed higher catalytic activity when used.

Язык: Английский

Процитировано

11

Chemoenzymatic Catalysis: Cooperativity Enables Opportunity DOI
Logan Hessefort, Lauren J. Harstad,

Kayla R. Merker

и другие.

ChemBioChem, Год журнала: 2023, Номер 24(14)

Опубликована: Май 30, 2023

The application of enzymes in synthetic organic chemistry has emerged as a powerful means to generate molecular complexity highly selective, efficient, and sustainable manner. While have increasingly been incorporated into sequences for numerous academic industrial applications on their own sequential processes, utility cooperative catalysis with small molecule catalytic platforms recently drawn increased attention across the field synthesis. In this review, we present selection notable accomplishments chemoenzymatic provide perspective its future directions.

Язык: Английский

Процитировано

11

Recent Advances in the Use of 2‐Aminobenzyl Alcohols in the Synthesis of Quinolines, Quinazolines and Other N‐Heterocycles DOI
Fatemeh Doraghi,

Farzad Gilaninezhad,

Somaye Karimian

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(10), С. 2142 - 2164

Опубликована: Янв. 17, 2024

Abstract N‐Heterocyclic compounds, in particular, quinolines and quinazolines are frequently used medicinal chemistry. Therefore, the direct clean synthesis of these valuable scaffolds has been a great interest for many years. 2‐Aminobenzyl alcohols as an alternative reactant instead unstable expensive 2‐aminobenzaldehydes can be construction N‐fused heterocycles including quinolines, quinazolines, oxazines, thiazines, selenazines, imidazoles, diazepines, etc. In this review article, we have discussed recent developments use 2‐aminobenzyl diverse heterocycles.

Язык: Английский

Процитировано

4

CuO NPs catalyzed synthesis of quinolines, pyridines, and pyrroles via dehydrogenative coupling strategy DOI
Shivangi Gupta, Ankur Maji, Dibyajyoti Panja

и другие.

Journal of Catalysis, Год журнала: 2022, Номер 413, С. 1017 - 1027

Опубликована: Авг. 13, 2022

Язык: Английский

Процитировано

18

Well-defined manganese complex catalyzed dehydrogenative synthesis of quinazolin-4(3H)-ones and 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxides DOI

Debjyoti Pal,

Avijit Mondal, Dipankar Srimani

и другие.

Catalysis Science & Technology, Год журнала: 2022, Номер 12(10), С. 3202 - 3208

Опубликована: Янв. 1, 2022

The synthesis of N-heterocycles has been considered an emerging topic chemical research due to its widespread usage in medicinal chemistry, materials science, and natural product synthesis.

Язык: Английский

Процитировано

18

Nickel-catalyzed sustainable synthesis of N-heterocycles through dehydrogenative coupling of alcohols DOI

Krishanu Bera,

Arup Mukherjee

Tetrahedron Letters, Год журнала: 2021, Номер 81, С. 153326 - 153326

Опубликована: Авг. 20, 2021

Язык: Английский

Процитировано

21

RuII-Complexes of heteroditopic chelating NHC ligands: effective catalysts for the β-alkylation of secondary alcohols and the synthesis of 2-alkylaminoquinoline derivatives following the dehydrogenative protocol DOI
Vivek Kumar Singh, S. N. R. Donthireddy,

Vipin K. Pandey

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2022, Номер 20(9), С. 1945 - 1951

Опубликована: Янв. 1, 2022

Ru II -Complexes of a heteroditopic NHC ligand, featuring ImNHC and tzNHC donors, were noted to be very efficient catalysts (up 0.001 mol%) for β-alkylation secondary alcohols one pot synthesis diverse 2-alkylaminoquinoline derivatives.

Язык: Английский

Процитировано

16

Lemon Juice: A Versatile Biocatalyst and Green Solvent in Organic Transformations DOI
Baji Baba Shaik, Pule Seboletswe, Sachin Balaso Mohite

и другие.

ChemistrySelect, Год журнала: 2022, Номер 7(5)

Опубликована: Фев. 1, 2022

Abstract Green chemistry is the basis for fast‐growing, eco‐friendly, alternative sustainable technologies development of chemical products without use or generation hazardous catalysts. The role naturally occurring fruit juice as a catalyst solvent in organic synthesis has gained focused interest across globe. Lemon juice‐mediated been widely explored recently highly significant, selective and biocatalyst synthesis. This review presents recent developments on lemon‐juice mediated transformations their application to synthesize molecules building blocks pharmaceutical interest. We believe this article will be researchers both academic industrial settings developing novel pharmacophores from green principles perspective.

Язык: Английский

Процитировано

15