Enriching calixarene functionality with 1,3-diketone groups-Reference-Cited by-同舟云学术

Enriching calixarene functionality with 1,3-diketone groups

Published:2023 Issue:14 Volume:10 Page:3619-3636
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Sakovich Maria¹,Sokolova Daria¹^ORCID,Alekseev Ivan¹^ORCID,Lentin Ivan¹^ORCID,Gorbunov Alexander¹^ORCID,Malakhova Maria¹^ORCID,Ershov Ivan¹^ORCID,Zairov Rustem²³^ORCID,Korniltsev Ilia¹^ORCID,Podyachev Sergey¹²^ORCID,Bezzubov Stanislav⁴^ORCID,Kovalev Vladimir¹^ORCID,Vatsouro Ivan¹^ORCID

Affiliation:

1. Department of Chemistry, M. V. Lomonosov Moscow State University, Lenin's Hills 1, 119991 Moscow, Russia

2. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzov str. 8, 420088 Kazan, Russia

3. Aleksander Butlerov Institute of Chemistry, Kazan Federal University, Lobachevskogo str. 1/29, 420008 Kazan, Russia

4. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Leninskii pr. 31, 119991 Moscow, Russia

Abstract

Diverse calixarene 1,3-diketones including those having additional triazole or crown ether functionalities can be readily prepared by acylation of magnesium enolates of acetophenones with calixarene-based 1-acylbenzotriazoles.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00759F

Reference59 articles.

1. Luminous lanthanide diketonates: Review on synthesis and optoelectronic characterizations

2. Recent Developments in the Synthesis of β-Diketones

3. β‐Diketones as Scaffolds for Anticancer Drug Design – From Organic Building Blocks to Natural Products and Metallodrug Components