Stasiak J, Woerpel K
Org Lett. 2025; 27(9):2037-2041.
PMID: 40009755
PMC: 11894669.
DOI: 10.1021/acs.orglett.4c04629.
Badalamenti N, Maggio A, Fontana G, Bruno M, Lauricella M, DAnneo A
Int J Mol Sci. 2024; 25(7).
PMID: 38612735
PMC: 11011390.
DOI: 10.3390/ijms25073925.
Mushtaq A, Zahoor A
RSC Adv. 2023; 13(47):32975-33027.
PMID: 38025859
PMC: 10631541.
DOI: 10.1039/d3ra05058k.
Hennessy M, Gandhi H, OSullivan T
Molecules. 2023; 28(11).
PMID: 37298799
PMC: 10254861.
DOI: 10.3390/molecules28114317.
Ahmed A, Dai C, Kuo Y, Sheu J
Metabolites. 2023; 13(3).
PMID: 36984832
PMC: 10056678.
DOI: 10.3390/metabo13030392.
Stereodivergent Total Syntheses of (+)-Mycaperoxides C, D, G Methyl Ester and (-)-Mycaperoxide B.
Kerim M, Evanno L, Ferrie L
Chemistry. 2022; 29(6):e202203004.
PMID: 36305658
PMC: 10107902.
DOI: 10.1002/chem.202203004.
Dissecting the Mechanism of the Nonheme Iron Endoperoxidase FtmOx1 Using Substrate Analogues.
Zhu G, Yan W, Wang X, Cheng R, Naowarojna N, Wang K
JACS Au. 2022; 2(7):1686-1698.
PMID: 35911443
PMC: 9326825.
DOI: 10.1021/jacsau.2c00248.
New synthesis of tetraoxaspirododecane-diamines and tetraoxazaspirobicycloalkanes.
Makhmudiyarova N, Shangaraev K, Dzhemileva L, Tyumkina T, Mescheryakova E, Dyakonov V
RSC Adv. 2022; 9(51):29949-29958.
PMID: 35531552
PMC: 9072112.
DOI: 10.1039/c9ra06372b.
Molecular insights into the endoperoxide formation by Fe(II)/α-KG-dependent oxygenase NvfI.
Mori T, Zhai R, Ushimaru R, Matsuda Y, Abe I
Nat Commun. 2021; 12(1):4417.
PMID: 34285212
PMC: 8292354.
DOI: 10.1038/s41467-021-24685-6.
Hydroperoxidations of Alkenes using Cobalt Picolinate Catalysts.
Peralta-Neel Z, Woerpel K
Org Lett. 2021; 23(13):5002-5006.
PMID: 34125543
PMC: 9022486.
DOI: 10.1021/acs.orglett.1c01489.
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity.
Dembitsky V, Ermolenko E, Savidov N, Gloriozova T, Poroikov V
Molecules. 2021; 26(3).
PMID: 33525706
PMC: 7865715.
DOI: 10.3390/molecules26030686.
Synthesis of Enantiopure Triols from Racemic Baylis-Hillman Adducts Using a Diastereoselective Peroxidation Reaction.
Zuckerman D, Woerpel K
Org Lett. 2020; 22(22):9075-9080.
PMID: 33141576
PMC: 7680403.
DOI: 10.1021/acs.orglett.0c03439.
Diastereoselective peroxidation of derivatives of Baylis-Hillman adducts.
Zuckerman D, Woerpel K
Tetrahedron. 2020; 75(31):4118-4129.
PMID: 32831414
PMC: 7437930.
DOI: 10.1016/j.tet.2019.05.008.
First Example of Catalytic Synthesis of Cyclic S-Containing Di- and Triperoxides.
Makhmudiyarova N, Ishmukhametova I, Dzhemileva L, Dyakonov V, Ibragimov A, Dzhemilev U
Molecules. 2020; 25(8).
PMID: 32325665
PMC: 7221664.
DOI: 10.3390/molecules25081874.
Hydrogen Donation but not Abstraction by a Tyrosine (Y68) during Endoperoxide Installation by Verruculogen Synthase (FtmOx1).
Dunham N, Del Rio Pantoja J, Zhang B, Rajakovich L, Allen B, Krebs C
J Am Chem Soc. 2019; 141(25):9964-9979.
PMID: 31117657
PMC: 6901024.
DOI: 10.1021/jacs.9b03567.
Synthesis of Novel -Kaurane-Type Diterpenoid Derivatives Effective for Highly Aggressive Tumor Cells.
Hu Y, Li X, Ma Z, Puno P, Zhao Y, Zhao Y
Molecules. 2018; 23(12).
PMID: 30563165
PMC: 6321055.
DOI: 10.3390/molecules23123216.
New Cembranoids and a Biscembranoid Peroxide from the Soft Coral .
Peng C, Huang C, Ahmed A, Hwang T, Dai C, Sheu J
Mar Drugs. 2018; 16(8).
PMID: 30082637
PMC: 6117711.
DOI: 10.3390/md16080276.
Novofumigatonin biosynthesis involves a non-heme iron-dependent endoperoxide isomerase for orthoester formation.
Matsuda Y, Bai T, Phippen C, Nodvig C, Kjaerbolling I, Vesth T
Nat Commun. 2018; 9(1):2587.
PMID: 29968715
PMC: 6030086.
DOI: 10.1038/s41467-018-04983-2.
Terpenoids from the Soft Coral sp. Collected in Yongxing Island.
Qin G, Tang X, Sun Y, Luo X, Zhang J, van Ofwegen L
Mar Drugs. 2018; 16(4).
PMID: 29652789
PMC: 5923414.
DOI: 10.3390/md16040127.
Peroxides with Anthelmintic, Antiprotozoal, Fungicidal and Antiviral Bioactivity: Properties, Synthesis and Reactions.
A Vil V, Yaremenko I, Ilovaisky A, Terentev A
Molecules. 2017; 22(11).
PMID: 29099089
PMC: 6150334.
DOI: 10.3390/molecules22111881.
