@article{oai:kanagawa-u.repo.nii.ac.jp:00002929,
 author = {佐藤, 憲一 and Sato, Ken-ichi and Kajihara, Yasuhiro and Nakamura, Yutaka and Yoshimura, Juji},
 issue = {9},
 journal = {Chemistry Letters},
 month = {},
 note = {Oxidation of 1L-(1,2,3′,4,5/3,6)-3-hydroxymethyl-2,4,5-tri-O-methoxymethyl-3,3′-O-methylene-6-nitro-2,3,4,5-tetrahydroxycyclohexanecarbaldehyde dimethyl acetal with potassium t-butoxide and m-chloroperbenzoic acid has given corresponding carbonyl derivative in 65% yield. The carbonyl compound has been successfully converted into the desired key compound for tetrodotoxin synthesis in excellent yield via the spiro α-chloro-epoxide derivative., Article},
 pages = {1559--1562},
 title = {Synthesis of the Functionalized Cyclohexanecarbaldehyde Derivative. A Potential Key Compound for Total Synthesis of Optically Active Tetrodotoxin},
 volume = {20},
 year = {1991}
}