Eiseman, J. L.; Bai, L.; Jung W.-H.; Moura-Letts, G.; Day, B. W.; Curran, D. P. (2008). “Improved Synthesis of 6-epi-Dictyostatin and Antitumor Efficacy in Mice Bearing MDA-MB231 Human Breast Cancer Xenografts”. J. Med. Chem.51 (21): 6650. doi:10.1021/jm800979v.
Nicolaou, K. C.; Baker, T. M.; Nakamura, T. (2011). “Synthesis of the WXYZA′ Domain of Maitotoxin”. J. Am. Chem. Soc.133 (2): 220. doi:10.1021/ja109533y.
Müller, S.; Mayer, T.; Sasse, F.; Maier, M. E. (2011). “Synthesis of a Pladienolide B Analogue with the Fully Functionalized Core Structure”. Org. Lett.13 (15): 3940. doi:10.1021/ol201464m.
Yamamoto, A.; Ueda, A.; Brémond, P.; Tiseni, P. S.; Kishi, Y. (2012). “Total Synthesis of Halichondrin C”. J. Am. Chem. Soc.134 (2): 893. doi:10.1021/ja2108307.
Ueda, A.; Yamamoto, A.; Kato, D.; Kishi, Y. (2014). “Total Synthesis of Halichondrin A, the Missing Member in the Halichondrin Class of Natural Products”. J. Am. Chem. Soc.136 (13): 5171. doi:10.1021/ja5013307.
Beveridge, R. E.; Batey, R. A. (2014). “An Organotrifluoroborate-Based Convergent Total Synthesis of the Potent Cancer Cell Growth Inhibitory Depsipeptides Kitastatin and Respirantin”. Org. Lett.16 (9): 2322. doi:10.1021/ol500484f.
Janetzko, J.; Batey, R. A. (2014). “Organoboron-Based Allylation Approach to the Total Synthesis of the Medium-Ring Dilactone (+)-Antimycin A1b”. J. Org. Chem.79 (16): 7415. doi:10.1021/jo501134d.
Wünsch, S.; Breit, B. (2015). “Probing o-Diphenylphosphanyl Benzoate (o-DPPB)-Directed C-C Bond Formation: Total Synthesis of Dictyostatin”. Chem. Eur. J.21 (6): 2358. doi:10.1002/chem.201406252.
Goodreid, J. D.; Da Silveira Dos Santos, E.; Batey, R. A. (2015). “A Lanthanide(III) Triflate Mediated Macrolactonization/Solid-Phase Synthesis Approach for Depsipeptide Synthesis”. Org. Lett.17 (9): 2182. doi:10.1021/acs.orglett.5b00781.
Ogawa, H.; Iwasaki, A.; Sumimoto, S.; Iwatsuki, M.; Ishiyama, A.; Hokari, R.; Otoguro, K.; Omura, S. et al. (2017). “Isolation and Total Synthesis of Hoshinolactam, an Antitrypanosomal Lactam from a Marine Cyanobacterium”. Org. Lett.19 (4): 890. doi:10.1021/acs.orglett.7b00047.
Yahata, K.; Ye, N.; Iso, K.; Naini, S. R.; Yamashita, S.; Ai, Y.; Kishi, Y. (2017). “Unified Synthesis of Right Halves of Halichondrins A–C”. J. Org. Chem.82 (17): 8792. doi:10.1021/acs.joc.7b01283.
Shiina, I.; Ibuka, R.; Kubota, M. (2002). “A New Condensation Reaction for the Synthesis of Carboxylic Esters from Nearly Equimolar Amounts of Carboxylic Acids and Alcohols Using 2-Methyl-6-nitrobenzoic Anhydride”. Chem. Lett.31 (3): 286. doi:10.1246/cl.2002.286.
Shiina, I.; Hashizume, M.; Yamai, Y.; Oshiumi, H.; Shimazaki, T.; Takasuna, Y.; Ibuka, R. (2005). “Enantioselective Total Synthesis of Octalactin A Using Asymmetric Aldol Reactions and a Rapid Lactonization To Form a Medium-Sized Ring”. Chem. Eur. J.11: 6601–6608. doi:10.1002/chem.200500417. PMID16118824.
Shiina, I. (2014). “An Adventurous Synthetic Journey with MNBA from Its Reaction Chemistry to the Total Synthesis of Natural Products”. Bull. Chem. Soc. Jpn.87 (2): 196. doi:10.1246/bcsj.20130216.
Shiina, I.; Hashizume, M.; Yamai, Y.; Oshiumi, H.; Shimazaki, T.; Takasuna, Y.; Ibuka, R. (2005). “Enantioselective Total Synthesis of Octalactin A Using Asymmetric Aldol Reactions and a Rapid Lactonization To Form a Medium-Sized Ring”. Chem. Eur. J.11: 6601–6608. doi:10.1002/chem.200500417. PMID16118824.