10) Y. Goda, K. Sakamoto, K. Murata, H. Fuwa, Total synthesis and biological evaluation of (−)-enigmazole B, Bulletin of the Chemical Society of Japan, 2025, 98, uoaf079.
 
9) K. Ohyama,‡ T. Masuda,‡ K. Sakamoto, A. Yoshimura, K. Tatsumoto, K. Murata, H. Fuwa, Total Synthesis of (−)-Enigmazole A by the Macrocyclization/Transannular Pyran Cyclization Strategy: Application to Structure–Activity Relationship Investigations, The Journal of Organic Chemistry, 2025, 90, 10500-10514.
 
8) Murakami, R.; Mori, T.; Murata, K.: Fuwa, H., 
Total Synthesis of Exiguolide Stereoisomers: Impact of Stereochemical Permutation on Reactivity, Conformation, and Biological Activity, The Journal of Organic Chemistry, 2025, 90, 753–767.
 
7) Obana, T.; Nakajima, M.; Nakazato, K.; Nakagawa, H.; Murata, K.; Tsuda, M.; Fuwa, H., Iriomoteolide-1a and -1b: Structure Elucidation by Integrating NMR Spectroscopic Analysis, Theoretical Calculation, and Total Synthesis, Journal of the American Chemical Society, 2024, 146, 29836–29846.
 
6) Minami, R.; Kasai, T.; Murata, K.: Fuwa, H.,
Total Synthesis of (+)-Muricatetrocin B via a Late-Stage Co-Catalyzed Hartung–Mukaiyama Cyclization, Organic Letters, 2023, 25, 5745–5749.
 
5) Murata, K.; Mori, H.; Fuwa, H., GIAO NMR Calculation-driven Stereochemical Assignment of Marine Macrolide Natural Products: Assessment of the Performance of DP4 and DP4+ Analyses and Assignment of the Relative Configuration of Leptolyngbyalide A–C/Oscillariolide Macrolactone, Bull. Chem. Soc. Jpn.2022, 95, 1775–1785.
 
4) Murata, K.; Minami, R.; Fuwa, H., Asymmetric Synthesis of (−)-Atorvastatin Calcium by Tandem Catalysis, Bulletin of the Chemical Society of Japan, 2021, 94, 2028–2035.
 
3) 村田佳亮, 不破春彦, タンデム反応と複雑天然物の全合成, 化学工業特集天然物化学の新展開, 2020, 71（2）, 117–124.
 
2) Murata, K.; Takeshita, H.; Sakamoto, K.; Fuwa, H., Tandem Three-Component Synthesis of Syn-1,2- and Syn-1,3-Diol Derivatives, Chemistry - An Asian Journal, 2020, 15, 807–819.
 
1) Murata, K.; Sakamoto, K.; Fuwa, H., Stereoselective Tandem Synthesis of Syn-1,3-Diol Derivatives by Integrating Olefin Cross-Metathesis, Hemiacetalization, and Intramolecular Oxa-Michael Addition, Organic Letters, 2019, 21, 3730–3734