Computational assessments of diastereoselective [4+2] cycloaddition and 1,3-borotopic shift of a dearomatized tertiary boronic ester intermediate: reactivities explained through transition-state distortion energies.


Journal

RSC advances
ISSN: 2046-2069
Titre abrégé: RSC Adv
Pays: England
ID NLM: 101581657

Informations de publication

Date de publication:
23 Jul 2019
Historique:
received: 21 05 2019
accepted: 15 07 2019
entrez: 6 5 2022
pubmed: 26 7 2019
medline: 26 7 2019
Statut: epublish

Résumé

Interception of a dearomatized tertiary boronic ester, formed through a kinetically and thermodynamically favorable 1,2-metalate rearrangement/

Identifiants

pubmed: 35514518
doi: 10.1039/c9ra03820e
pii: c9ra03820e
pmc: PMC9067249
doi:

Types de publication

Journal Article

Langues

eng

Pagination

23148-23155

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Aqeel A Hussein (AA)

Faculty of Dentistry, University of Al-Ameed Karbala P.O. No: 198 Iraq.
Department of Chemistry, University of Southampton Southampton Hampshire SO17 1BJ UK aahh1f19@soton.ac.uk.

Faisal A Almalki (FA)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Umm Al-Qura University Makkah 21955 Saudi Arabia.

Alaa M Alqahtani (AM)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Umm Al-Qura University Makkah 21955 Saudi Arabia.

Sergey Shityakov (S)

Department of Anesthesia and Critical Care, University of Würzburg 97080 Würzburg Germany.

Classifications MeSH