A Four-step Synthesis of the Hydroazulene Core of Guanacastepene
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[reaction: see text] A concise, four-step conversion of 2-methylcyclopentenone to hydroazulene 2 is described. An alternative approach that led to an unexpected [5,5]-bicyclic carbon framework is also discussed.
Electrochemically Enabled Total Syntheses of Natural Products.
Hatch C, Chain W ChemElectroChem. 2023; 10(11).
PMID: 38106361 PMC: 10723087. DOI: 10.1002/celc.202300140.
Application of Pauson-Khand reaction in the total synthesis of terpenes.
Heravi M, Mohammadi L RSC Adv. 2022; 11(61):38325-38373.
PMID: 35493249 PMC: 9044263. DOI: 10.1039/d1ra05673e.
Zhang F, Feng T J Fungi (Basel). 2022; 8(3).
PMID: 35330246 PMC: 8951520. DOI: 10.3390/jof8030244.
Synthetic efforts toward the bicyclo[3.2.1]octane fragment of rhodojaponin III.
Webster C, Park H, Ennis A, Hong J Tetrahedron Lett. 2021; 71.
PMID: 34054153 PMC: 8153367. DOI: 10.1016/j.tetlet.2021.153055.
Four-Step Total Synthesis of (+)-Yaoshanenolides A and B.
Thorat S, Palange M, Kontham R ACS Omega. 2019; 3(6):7036-7045.
PMID: 31458866 PMC: 6644681. DOI: 10.1021/acsomega.8b00701.