2021
DOI: 10.1002/tcr.202100206
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Transition Metal/Lewis Acid Catalyzed Reactions of Zerumbone for Diverse Molecular Motifs

Abstract: Zerumbone is a naturally occurring humulene type sesquiterpene, isolated from the rhizomes of Zingiber zerumbet (L.) Smith with excellent therapeutic potential and is recognized as a valuable synthon for the construction of diverse array of natural product motifs. In this review, we intended to highlight our achievements in utilizing abundant natural product zerumbone and its derivatives for the development of pharmacologically relevant molecular scaffolds. We provided an account of the transition‐metal cataly… Show more

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Cited by 3 publications
(1 citation statement)
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“…In addition, bio-isosteric replacements in the ortho position of the phenyl ring of zerumbone led to a series of new hydrazones, including 5a-f and 9a-f, with confirmed cytotoxic effects against three human cancer cell lines, HepG-2, SK-LU-1, and MCF-7 [ 111 ]. Another derivative, zerumbone epoxide, results from numerous reactions triggered by transition metal/Lewis acid-catalysed 1,4-conjugate addition of zerumbone [ 113 ].…”
Section: Zerumbone Derivativementioning
confidence: 99%
“…In addition, bio-isosteric replacements in the ortho position of the phenyl ring of zerumbone led to a series of new hydrazones, including 5a-f and 9a-f, with confirmed cytotoxic effects against three human cancer cell lines, HepG-2, SK-LU-1, and MCF-7 [ 111 ]. Another derivative, zerumbone epoxide, results from numerous reactions triggered by transition metal/Lewis acid-catalysed 1,4-conjugate addition of zerumbone [ 113 ].…”
Section: Zerumbone Derivativementioning
confidence: 99%