Three-component reaction of azulene, aryl glyoxal and 1,3-dicarbonyl compound for the synthesis of various azulene derivatives

Jing Gong; Anatoly A. Peshkov; Jiafeng Yu; Sagadat Amandykova; Aidana Gimnkhan; Jianjun Huang; Stepan Kashtanov; Olga P. Pereshivko; Vsevolod A. Peshkov

doi:10.1039/d0ra00356e

Three-component reaction of azulene, aryl glyoxal and 1,3-dicarbonyl compound for the synthesis of various azulene derivatives

Jing Gong, Anatoly A. Peshkov, Jiafeng Yu, Sagadat Amandykova, Aidana Gimnkhan, Jianjun Huang, Stepan Kashtanov, Olga P. Pereshivko^*, Vsevolod A. Peshkov

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

A three-component reaction of an azulene, an aryl glyoxal and a 1,3-dicarbonyl compound has been elaborated to access a series of azulene derivatives. Some of these azulene-containing adducts were further subjected to post-MCR transformations to assemble azulene-heterocycle conjugates.

Original language	English (US)
Pages (from-to)	10113-10117
Number of pages	5
Journal	RSC ADVANCES
Volume	10
Issue number	17
DOIs	https://doi.org/10.1039/d0ra00356e
State	Published - Mar 10 2020

Bibliographical note

Funding Information:
This work was supported by the start-up fund from Soochow University (grant Q410900714), National Natural Science Foundation of China (grant 21650110445), Natural Science Foundation of Jiangsu Province of China (grant BK20160310), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientic and Technologic Infrastructure of Suzhou (grant SZS201708) and the Social Policy Grant of Nazarbayev University.

Funding Information:
This work was supported by the start-up fund from Soochow University (grant Q410900714), National Natural Science Foundation of China (grant 21650110445), Natural Science Foundation of Jiangsu Province of China (grant BK20160310), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientific and Technologic Infrastructure of Suzhou (grant SZS201708) and the Social Policy Grant of Nazarbayev University.

Publisher Copyright:
This journal is © The Royal Society of Chemistry.

ASJC Scopus subject areas

General Chemistry
General Chemical Engineering

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title = "Three-component reaction of azulene, aryl glyoxal and 1,3-dicarbonyl compound for the synthesis of various azulene derivatives",

abstract = "A three-component reaction of an azulene, an aryl glyoxal and a 1,3-dicarbonyl compound has been elaborated to access a series of azulene derivatives. Some of these azulene-containing adducts were further subjected to post-MCR transformations to assemble azulene-heterocycle conjugates.",

author = "Jing Gong and Peshkov, {Anatoly A.} and Jiafeng Yu and Sagadat Amandykova and Aidana Gimnkhan and Jianjun Huang and Stepan Kashtanov and Pereshivko, {Olga P.} and Peshkov, {Vsevolod A.}",

note = "Funding Information: This work was supported by the start-up fund from Soochow University (grant Q410900714), National Natural Science Foundation of China (grant 21650110445), Natural Science Foundation of Jiangsu Province of China (grant BK20160310), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientic and Technologic Infrastructure of Suzhou (grant SZS201708) and the Social Policy Grant of Nazarbayev University. Funding Information: This work was supported by the start-up fund from Soochow University (grant Q410900714), National Natural Science Foundation of China (grant 21650110445), Natural Science Foundation of Jiangsu Province of China (grant BK20160310), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientific and Technologic Infrastructure of Suzhou (grant SZS201708) and the Social Policy Grant of Nazarbayev University. Publisher Copyright: This journal is {\textcopyright} The Royal Society of Chemistry.",

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month = mar,

day = "10",

doi = "10.1039/d0ra00356e",

language = "English (US)",

volume = "10",

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AU - Gong, Jing

AU - Peshkov, Anatoly A.

AU - Yu, Jiafeng

AU - Amandykova, Sagadat

AU - Gimnkhan, Aidana

AU - Huang, Jianjun

AU - Kashtanov, Stepan

AU - Pereshivko, Olga P.

AU - Peshkov, Vsevolod A.

N1 - Funding Information: This work was supported by the start-up fund from Soochow University (grant Q410900714), National Natural Science Foundation of China (grant 21650110445), Natural Science Foundation of Jiangsu Province of China (grant BK20160310), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientic and Technologic Infrastructure of Suzhou (grant SZS201708) and the Social Policy Grant of Nazarbayev University. Funding Information: This work was supported by the start-up fund from Soochow University (grant Q410900714), National Natural Science Foundation of China (grant 21650110445), Natural Science Foundation of Jiangsu Province of China (grant BK20160310), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientific and Technologic Infrastructure of Suzhou (grant SZS201708) and the Social Policy Grant of Nazarbayev University. Publisher Copyright: This journal is © The Royal Society of Chemistry.

PY - 2020/3/10

Y1 - 2020/3/10

N2 - A three-component reaction of an azulene, an aryl glyoxal and a 1,3-dicarbonyl compound has been elaborated to access a series of azulene derivatives. Some of these azulene-containing adducts were further subjected to post-MCR transformations to assemble azulene-heterocycle conjugates.

AB - A three-component reaction of an azulene, an aryl glyoxal and a 1,3-dicarbonyl compound has been elaborated to access a series of azulene derivatives. Some of these azulene-containing adducts were further subjected to post-MCR transformations to assemble azulene-heterocycle conjugates.

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ER -

Three-component reaction of azulene, aryl glyoxal and 1,3-dicarbonyl compound for the synthesis of various azulene derivatives

Abstract

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