On the proposed structures and stereocontrolled synthesis of the cephalosporolides

Scholarly Works

• Xochicale-Santana, L.; Cortezano-Arellano, O.; Frontana-Uribe, B. A.; Jimenez-Pérez, V. M.; Sartillo-Piscil, F. The Stereoselective Total Synthesis of the Elusive Cephalosporolide F. The Journal of organic chemistry 2023, 88, 4880–4885. doi:10.1021/acs.joc.3c00251
• Ota, K.; Miyaoka, H.; Kamaike, K. Total Synthesis and Structural Revision of Cephalosporolide J. Synlett 2022, 34, 271–276. doi:10.1055/a-1967-1284
• Yao, H.; Wang, J.; Tong, R. Recent Developments in Total Syntheses of Cephalosporolides, Penisporolides, and Ascospiroketals. Chemical record (New York, N.Y.) 2017, 17, 1109–1123. doi:10.1002/tcr.201700001
• Wang, J.; Tong, R. A NMR method for relative stereochemical assignments of the tricyclic core of cephalosporolides, penisporolides and related synthetic analogues. Organic Chemistry Frontiers 2017, 4, 140–146. doi:10.1039/c6qo00556j
• Halle, M. B.; Fernandes, R. A. Total Synthesis of Marine Natural Products: Cephalosporolides. Asian Journal of Organic Chemistry 2016, 5, 839–854. doi:10.1002/ajoc.201600208
• Wang, J.; Tong, R. Total Synthesis of Purported Cephalosporolides H and I, Penisporolide B, and Their Stereoisomers. The Journal of organic chemistry 2016, 81, 4325–4339. doi:10.1021/acs.joc.6b00788
• Wang, J.; Tong, R. Asymmetric Total Syntheses of ent-Ascospiroketals A and B. Organic letters 2016, 18, 1936–1939. doi:10.1021/acs.orglett.6b00796
• Raghavan, S.; Patel, J. S.; Ramakrishna, K. Synthesis of (−) cephalosporolide E and (+) cephalosporolide F utilizing the vinylogous Mukaiyama type reaction with an α-chloro sulfide. RSC Advances 2016, 6, 72877–72884. doi:10.1039/c6ra13861f
• Chang, S.; Hur, S.; Britton, R. Total Synthesis and Configurational Assignment of Ascospiroketal A. Chemistry (Weinheim an der Bergstrasse, Germany) 2015, 21, 16646–16653. doi:10.1002/chem.201502754
• Li, J.; Zhao, C.; Liu, J.; Du, Y. Total synthesis of proposed cephalosporolides H and I. Tetrahedron 2015, 71, 3885–3889. doi:10.1016/j.tet.2015.04.025
• Thota, G. K.; Tarigopula, C.; Balamurugan, R. Tandem activation by gold: synthesis of dioxolanes by intermolecular reaction of epoxides and alkynes in acetone. Tetrahedron 2015, 71, 2280–2289. doi:10.1016/j.tet.2015.02.040
• Cortezano-Arellano, O.; Quintero, L.; Sartillo-Piscil, F. Total synthesis of cephalosporolide E via a tandem radical/polar crossover reaction. The use of the radical cations under nonoxidative conditions in total synthesis. The Journal of organic chemistry 2015, 80, 2601–2608. doi:10.1021/jo502757c
• Chaudhari, D. A.; Kattanguru, P.; Fernandes, R. A. A concise protecting-group-free synthesis of cephalosporolides E and F. RSC Advances 2015, 5, 42131–42134. doi:10.1039/c5ra06991b
• Chang, S.; Hur, S.; Britton, R. Total Synthesis of Ascospiroketal A Through a AgI‐Promoted Cyclization Cascade. Angewandte Chemie (International ed. in English) 2014, 54, 211–214. doi:10.1002/anie.201408905
• Chang, S.; Hur, S.; Britton, R. Total Synthesis of Ascospiroketal A Through a AgI‐Promoted Cyclization Cascade. Angewandte Chemie 2014, 127, 213–216. doi:10.1002/ange.201408905
• Kona, C. N.; Ramana, C. V. Total synthesis of naturally occurring cephalosporolides E/F. Tetrahedron 2014, 70, 3653–3656. doi:10.1016/j.tet.2014.04.026
• Blunt, J. W.; Copp, B. R.; Keyzers, R. A.; Munro, M. H. G.; Prinsep, M. R. Marine natural products. Natural product reports 2014, 31, 160. doi:10.1039/c3np70117d
• Finch, O. C.; Furkert, D. P.; Brimble, M. A. Synthesis of the spiroacetal core of the cephalosporolide family of natural products. Tetrahedron 2014, 70, 590–596. doi:10.1016/j.tet.2013.12.012
• Brimble, M. A.; Stubbing, L. A. Synthesis of 5,6- and 6,6-Spirocyclic Compounds. Synthesis of Saturated Oxygenated Heterocycles I 2013, 46, 189–267. doi:10.1007/978-3-642-41473-2_5
• Song, L.; Liu, Y.; Tong, R. Cephalosporolide B Serving as a Versatile Synthetic Precursor: Asymmetric Biomimetic Total Syntheses of Cephalosporolides C, E, F, G, and (4-OMe-)G. Organic letters 2013, 15, 5850–5853. doi:10.1021/ol402913m

Explore citations to this article at