A computational investigation towards substitution effects on 8π electrocyclisation of conjugated 1,3,5,7-octatetraenes-Reference-Cited by-同舟云学术

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A computational investigation towards substitution effects on 8π electrocyclisation of conjugated 1,3,5,7-octatetraenes

Published:2023 Issue:44 Volume:13 Page:30787-30797
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Arfan Nur Hazimah B. Z.¹,Hamid Malai Haniti S. A.¹^ORCID,Sheikh Nadeem S.¹^ORCID

Affiliation:

1. Chemical Sciences, Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, Gadong, BE1413, Brunei Darussalam

Abstract

Significance of quantum chemical calculations as a theoretical tool to identify the optimum substitution pattern for a rapid 8π-electrocyclisation of conjugated 1,3,5,7-octatetraene is presented.

Funder

Universiti Brunei Darussalam

Kementerian Pendidikan

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/RA/D3RA05127G

Reference52 articles.

1. Construction of Carbocycles from Methylenecyclopropanes

2. Organocatalytic Asymmetric Synthesis of Six-Membered Carbocycle-Based Spiro Compounds

3. Advances in the enantioselective synthesis of carbocyclic nucleosides

4. Recent Advances in the Total Synthesis of Natural Products Containing Eight-Membered Carbocycles (2009–2019)

5. Two-Phase Synthesis of Taxol

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