Year |
Citation |
Score |
2023 |
Li Z, Xu B, Alsup TA, Wei X, Ning W, Icenhour DG, Ehrenberger MA, Ghiviriga I, Giang BD, Rudolf JD. Cryptic Isomerization in Diterpene Biosynthesis and the Restoration of an Evolutionarily Defunct P450. Journal of the American Chemical Society. 145: 22361-22365. PMID 37813821 DOI: 10.1021/jacs.3c09446 |
0.667 |
|
2023 |
Wang Z, Yang Q, He J, Li H, Pan X, Li Z, Xu HM, Rudolf J, Tantillo D, Dong LB. Cytochrome P450 Mediated Cyclization in Eunicellane Derived Diterpenoid Biosynthesis. Angewandte Chemie (International Ed. in English). e202312490. PMID 37735947 DOI: 10.1002/anie.202312490 |
0.668 |
|
2023 |
Li Z, Rudolf JD. Biosynthesis, enzymology, and future of eunicellane diterpenoids. Journal of Industrial Microbiology & Biotechnology. PMID 37673680 DOI: 10.1093/jimb/kuad027 |
0.662 |
|
2023 |
Li Z, Xu B, Kojasoy V, Ortega T, Adpressa DA, Ning W, Wei X, Liu J, Tantillo DJ, Loesgen S, Rudolf JD. First -eunicellane terpene synthase in bacteria. Chem. 9: 698-708. PMID 36937101 DOI: 10.1016/j.chempr.2022.12.006 |
0.676 |
|
2021 |
Xu B, Li Z, Alsup TA, Ehrenberger MA, Rudolf JD. Bacterial diterpene synthases prenylate small molecules. Acs Catalysis. 11: 5906-5915. PMID 34796043 DOI: 10.1021/ACSCATAL.1C01113 |
0.683 |
|
2020 |
Rudolf JD, Alsup TA, Xu B, Li Z. Bacterial terpenome. Natural Product Reports. PMID 33169126 DOI: 10.1039/d0np00066c |
0.672 |
|
2019 |
Deng M, Zhang X, Li Z, Chen H, Zang S, Liang G. Rapid Construction of the Common [5-5-6] Tricyclic Ring Skeleton in Polycyclic Cembranoids and Norcembranoids via Intramolecular 1,3-Dipolar Cycloaddition. Organic Letters. PMID 30789271 DOI: 10.1021/acs.orglett.9b00285 |
0.589 |
|
2018 |
Xiang Y, Li Z, Wang LN, Yu ZX. TfOH- and HBF-Mediated Formal Cycloisomerizations and [4+3] Cycloadditions of Allene-alkynylbenzenes. The Journal of Organic Chemistry. PMID 30011205 DOI: 10.1021/Acs.Joc.8B00393 |
0.552 |
|
2015 |
Li Z, Geng Q, Lv Z, Pritchett BP, Baba K, Numajiri Y, Stoltz BM, Liang G. Selective syntheses of leuconolam, leuconoxine, and mersicarpine alkaloids from a common intermediate through regiocontrolled cyclizations by Staudinger reactionsâ Electronic supplementary information (ESI) available: Experimental details and procedures, compound characterization data, copies of (1)H and (13)C NMR spectra for new compounds. See DOI: 10.1039/c4qo00312hClick here for additional data file. Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry. 2: 236-240. PMID 25717379 DOI: 10.1039/C4Qo00312H |
0.549 |
|
2014 |
Lv Z, Li Z, Liang G. Total synthesis of mersicarpine through a cationic cyclization approach. Organic Letters. 16: 1653-5. PMID 24555758 DOI: 10.1021/ol500308e |
0.578 |
|
Show low-probability matches. |