A molecular electron density theory study of the mechanism, chemo- and stereoselectivity of the epoxidation reaction of R-carvone with peracetic acid-Reference-Cited by-同舟云学术

A molecular electron density theory study of the mechanism, chemo- and stereoselectivity of the epoxidation reaction of R-carvone with peracetic acid

Published:2019 Issue:49 Volume:9 Page:28500-28509
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Zeroual Abdellah¹²³⁴⁵^ORCID,Ríos-Gutiérrez Mar⁶⁷⁸⁹,Amiri Ouafa¹⁰¹¹¹²¹³⁵,El Idrissi Mohammed¹²³⁴⁵,Domingo Luis R.⁶⁷⁸⁹^ORCID

Affiliation:

1. Molecular Modeling and Spectroscopy Research Team

2. Faculty of Science

3. ChouaïbDoukkali University

4. 24000 El Jadida

5. Morocco

6. Department of Organic Chemistry

7. University of Valencia

8. Valencia

9. Spain

10. Laboratory of Organic and Analytical Chemistry

11. Faculty of Sciences and Techniques

12. Sultan Moulay Slimane University

13. Beni-Mellal

Abstract

The epoxidation reaction of R-carvone 8 with peracetic acid 9 has been studied within the molecular electron density theory at the B3LYP/6-311(d,p) computational level.

Funder

H2020 Marie Skłodowska-Curie Actions

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/RA/C9RA05309C

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5. An Isolable and Bench-Stable Epoxidizing Reagent Based on Triazine: Triazox

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