Curcumin‐based bioactive heterocycles derived via multicomponent reactions

Curcumin is an important phytochemical, found in the Asian countries, especially in the Indian subcontinent. The use of this “privileged natural product” in the diversity‐oriented synthesis of curcumin‐based heterocycles via multicomponent reactions (MCRs) is the subject of interest for many medicin...

Full description

Saved in:
Bibliographic Details
Published inArchiv der Pharmazie (Weinheim) Vol. 356; no. 8; pp. e2300171 - n/a
Main Authors Nagargoje, Amol A., Shaikh, Mubarak H., Shingate, Bapurao B.
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.08.2023
Subjects
Online AccessGet full text
ISSN0365-6233
1521-4184
1521-4184
DOI10.1002/ardp.202300171

Cover

Loading…
More Information
Summary:Curcumin is an important phytochemical, found in the Asian countries, especially in the Indian subcontinent. The use of this “privileged natural product” in the diversity‐oriented synthesis of curcumin‐based heterocycles via multicomponent reactions (MCRs) is the subject of interest for many medicinal chemists across the globe. This review particularly focuses on the reactions involving curcuminoids as one of the reactants in the MCRs of curcuminoid to synthesize curcumin‐based heterocycles. Also, the various pharmacological activities of curcumin‐based heterocycles generated via the MCR approach are discussed. The research work published in the last 10 years is in the focus of this review article. The use of curcumin as one of the reactants in various multicomponent reactions (MCR) yielded diverse curcumin‐based heterocycles. This review focuses on recent advances in the synthetic strategies and medicinal attributes of these MCR‐derived curcumin‐based heterocycles, surveying research articles published in the last 10 years.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ISSN:0365-6233
1521-4184
1521-4184
DOI:10.1002/ardp.202300171