Abstract
Tenuazonic acid derivatives were synthesized from amino acid esters by N-acetoacetylation with diketene followed by cyclization with sodium alkoxides. Some L-amino acid produced a small amount of DL-compounds in this process. N-Acetoacetyl group of diethyl aspartate cyclized to the α-ester group to form five-membered ring compound selectively. These compounds were condensed with carbonyl reagents. © 1967, The Pharmaceutical Society of Japan. All rights reserved.
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CITATION STYLE
Yuki, H., Tohira, Y., Aoki, B., Kano, T., Takama, S. I., & Yamazaki, T. (1967). Studies on Antiviral Agents. III.∗3 Synthesis of Tenuazonic Acid Derivatives. Chemical and Pharmaceutical Bulletin, 15(8), 1107–1111. https://doi.org/10.1248/cpb.15.1107
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