Showing posts with label Diels-Alder reaction. Show all posts
Showing posts with label Diels-Alder reaction. Show all posts

Thursday, 10 April 2025

A Comprehensive Overview of Cyclodextrins Catalyzed Diels-Alder Reactions | Chapter 3 | Chemical and Materials Sciences: Research Findings Vol. 2

Diels-Alder (DA) reactions typically yield heterocyclic six-membered ring compounds via a [4π+2π] cycloaddition of a diene (such as furan or cyclopentadiene) and a dienophile. The choice of solvent and catalyst is critical in affecting the yield and stereoselectivity of the reaction. Cyclodextrins, particularly beta-cyclodextrin (β-CD) and its derivatives, are commonly used as catalysts in aqueous medium due to their ability to form a favorable ternary complex with both the diene and dienophile. As a result, this paper summarizes several experimental studies on the catalytic effects of CDs on DA reactions, with an emphasis on yields, reaction durations, quantities, and selectivity. The first phase, reported by Ronald Breslow and colleagues in 1980, looked at the effect of inner cavity size on catalytic and inhibitory effects on DA processes. The following phase investigated the effect of cyclodextrin catalysts on endo- and stereoselectivity. Numerous studies have examined the potential of β-CD's interior size, derivatives, amounts, organic and aqueous media, and compatibility with the two reagents. In contrast, some research has concentrated on employing cyclodextrins as catalysts in Diels-Alder processes to generate large yields of bioactive chemicals and polymer synthesis under mild conditions, generally in aqueous solutions.

 

Author (s) Details

 

Amine Ez-zoubi
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques, Sidi Mohamed Ben Abdellah University, Route d’Imouzzer, Fez, Morocco.

 

Soukaina Benkirane
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques, Sidi Mohamed Ben Abdellah University, Route d’Imouzzer, Fez, Morocco.

 

Ayoub El-Mrabet
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques, Sidi Mohamed Ben Abdellah University, Route d’Imouzzer, Fez, Morocco.

 

Mouad Mouhsin
Laboratory of Engineering in Chemistry and Physics of Matter, Faculty of Science and Technologies, Sultan Moulay Slimane University, BP 523, Beni Mellal, Morocco.

 

Riham Sghyar
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques, Sidi Mohamed Ben Abdellah University, Route d’Imouzzer, Fez, Morocco and Equipe de Chimie Organique Appliquée à la valorisation des Ressources Naturelles et Protection de l’Environnement, Laboratoire de Chimie et Microbiologie Appliquées et Biotechnologies, FS, Abdelmalek Essaadi University Tetouan, Morocco.

 

Abdellatif Alami
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques, Sidi Mohamed Ben Abdellah University, Route d’Imouzzer, Fez, Morocco.

 

Chandrakant Sarode
Department of Chemistry, Bhusawal Arts, Science and P.O. Nahata Commerce College, Bhusawal, affiliated to KBC North Maharashtra University, Jalgaon, 425001, India.

 

Gaurav Gupta
Department of Chemistry, NTVS’s G.T.P. Arts, Commerce and Science College, Nandurbar, affiliated to KBC-North Maharashtra University, Jalgaon, 425001, India.

 

Abdellah Farah
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques, Sidi Mohamed Ben Abdellah University, Route d’Imouzzer, Fez, Morocco.

 

 

Please see the book here:- https://doi.org/10.9734/bpi/cmsrf/v2/4904

Tuesday, 28 July 2020

Biocide Chlorinated Compound for Inhibiting Sulfate Reducing Bacteria | Chapter 7 | Current Research and Development in Chemistry Vol.3


This chapter deals with biocides that can be used in sulfate reducing bacteria applications.
Preparation of bicyclic technologies containing chlorine atoms and/or ether groups in aromatic rings
can be regarded as a significant method for the construction of bicyclic systems and for the production
of additives. The Diels-Alder reaction (1,4 cycloaddition) is one of the most important forms of
cycloaddition reaction. Ether of the allylic type (dienophilic)
p-allyl bromo phenol was prepared and its
structure was proved by molecular weight, infrared spectra, refractive index, and density
determination. This adduct was obtained through the reaction of 1,4 cycloaddition of hexa chloro
cyclopentadiene (HCP) and the prepared dienophile. The reaction occurs without the use of solvent,
catalysts or any compound elimination. To determine the optimum conditions for the reaction, the
effect of variations in temperature, initial molar ratio and duration of reaction were studied. The
optimum conditions achieved were the recorded reaction temperature of 140°C, the initial molar ratio
diene: dienophile was 3:1 and the reaction time was 6 h. The maximum yield was 78% under these
optimum conditions. The prepared adduct as sulfate-reducing bacteria (SRB) confirmed very high
biological effect.

Author (s) Details

Azza M. Mazrouaa
Polymer Laboratory, Petrochemical Department, Egyptian Petroleum Research Institute, Nasr City, Cairo 11727, Egypt.

Mona A. Youssif
Polymer Laboratory, Petrochemical Department, Egyptian Petroleum Research Institute, Nasr City, Cairo 11727, Egypt.

Mohamed A. Shenashen
Polymer Laboratory, Petrochemical Department, Egyptian Petroleum Research Institute, Nasr City, Cairo 11727, Egypt.

Nahla A. Mansour
Polymer Laboratory, Petrochemical Department, Egyptian Petroleum Research Institute, Nasr City, Cairo 11727, Egypt.

View Book :-
http://bp.bookpi.org/index.php/bpi/catalog/book/217