2020
DOI: 10.1021/acs.orglett.0c00998
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Epoxy-Tethered Diels–Alder Reaction toward the Tricyclic Core of Kalihinols

Abstract: A chiral-template-driven intramolecular Diels–Alder reaction has been used to build the tricyclic core of kalihinols, a group of antimalarial marine natural products. The key starting materials are commercially available nerol and sulcatone.

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Cited by 4 publications
(2 citation statements)
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References 49 publications
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“…[ 10 ] Recently, a study displayed the reaction of an octadienol with 6‐me‐thyl‐5‐hepten‐2‐one to form an epoxide derivative. [ 11 ] All these reports show the synthesis of various epoxide analogues using some methods; however, some of these protocols require different conditions, among which are changes in temperature and pH. Analyzing these data, the objective of this research was to prepare two epoxy derivatives using some chemical reactions that do not require special conditions.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[ 10 ] Recently, a study displayed the reaction of an octadienol with 6‐me‐thyl‐5‐hepten‐2‐one to form an epoxide derivative. [ 11 ] All these reports show the synthesis of various epoxide analogues using some methods; however, some of these protocols require different conditions, among which are changes in temperature and pH. Analyzing these data, the objective of this research was to prepare two epoxy derivatives using some chemical reactions that do not require special conditions.…”
Section: Introductionmentioning
confidence: 99%
“…Reaction mechanism of a pyridine derivative (8) I G U R E 7 Preparation of chloroamide derivatives(10)(11)(12)(13)…”
mentioning
confidence: 99%