Revealing the Origin of Π‐facial and Regioselectivity in the Diels‐Alder Reaction of Unsymmetrical, Cage‐annulated 1,3‐Cyclohexadiene with Ethyl Propiolate Dienophile: a DFT Study-Reference-Cited by-同舟云学术

Revealing the Origin of Π‐facial and Regioselectivity in the Diels‐Alder Reaction of Unsymmetrical, Cage‐annulated 1,3‐Cyclohexadiene with Ethyl Propiolate Dienophile: a DFT Study

Published:2020-11-16 Issue:43 Volume:5 Page:13524-13529
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Patel Tulsi R.¹¹,Ganguly Bishwajit¹¹^ORCID

Affiliation:

1. Computation and Simulation Unit (Analytical & Environmental Science Division and Centralized Instrument Facility) CSIR-Central Salt & Marine Chemicals Research Institute, Bhavnagar, Gujarat, India- 364 002 Academy of Scientific and Innovative Research (AcSIR) Ghaziabad-201002 India

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202003443

Reference49 articles.

1. Catalytic asymmetric Diels Alder reactions

2. A Theoretical Investigation on the Regioselectivity of the Diels–Alder Cycloaddition of 9-(Methoxymethyl) Anthracene And Citraconic Anhydride

3. Influence of Non-Covalent Interactions in the Exo- and Regioselectivity of Aza-Diels–Alder Reactions: Experimental and DFT Calculations

4. Theoretical predication of Diels-Alder reactions of highly strained dienophiles

5. A theoretical study on the metal-free triazole formation through tandem [3+2] cycloaddition/retro-Diels-Alder reaction of benzyl azide and oxanorbornadienedicarboxylate

Cited by 1 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. Quantum mechanical modeling unveils the effect of substitutions on the activation barriers of the Diels–Alder reactions of an antiviral compound 7H-benzo[a]phenalene;Structural Chemistry;2022-05-10