Understanding the Intramolecular Diels-Alder Reactions of N-Substituted N-Allyl-Furfurylamines: An MEDT Study-Reference-Cited by-同舟云学术

Understanding the Intramolecular Diels-Alder Reactions of N-Substituted N-Allyl-Furfurylamines: An MEDT Study

Published:2017-10-23 Issue:30 Volume:2 Page:9736-9743
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Hallooman Dhanashree¹,Cudian Davina¹,Ríos-Gutiérrez Mar²,Rhyman Lydia¹³,Alswaidan Ibrahim A.⁴,Elzagheid Mohamed I.⁵,Domingo Luis R.²,Ramasami Ponnadurai¹³

Affiliation:

1. Computational Chemistry Group, Department of Chemistry; Faculty of Science, University of Mauritius; Réduit 80837 Mauritius

2. Department of Organic Chemistry; University of Valencia; Dr. Moliner 50 46100, Burjassot Valencia Spain

3. Department of Applied Chemistry; University of Johannesburg; Doornfontein Johannesburg 2028 South Africa

4. Department of Pharmaceutical Chemistry, College of Pharmacy; King Saud University; Riyadh 11451 Saudi Arabia

5. Department of Chemical and Process Engineering; Jubail Industrial College; Jubail Industrial City 31961 Saudi Arabia

Publisher

Wiley

Subject

General Chemistry

Reference30 articles.

1. 1967

2. The Diels-Alder reaction: an update

3. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

4. The Diels-Alder reaction: Selected practical methods 2001

5. 1991

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Investing in entropy: the strategy of cucurbit[n]urils to accelerate the intramolecular Diels–Alder cycloaddition reaction of tertiary furfuryl amines;Chemical Science;2024

2. Exploring the Mechanism of the Intramolecular Diels–Alder Reaction of (2E,4Z,6Z)-2(allyloxy)cycloocta-2,4,6-trien-1-one Using Bonding Evolution Theory;Molecules;2023-09-22

3. Understanding the regio-and diastereoselective synthesis of a potent antinociceptive isoxazolidine from C-(pyridin-3-yl)-N-phenylnitrone in the light of molecular electron density theory;Journal of the Serbian Chemical Society;2020

4. Alkylhalovinylboranes: a new class of Diels–Alder dienophiles;RSC Advances;2018