Chiral Synthesis of the BC-Ring System of Ciguatoxin from D-Glucose

Article abstract of DOI:10.1271/bbb.61.2019

The BC-ring system of ciguatoxin was stereoselectively synthesized by 12 steps from methyl α-D-glucopyranoside.

Full text of DOI:10.1271/bbb.61.2019

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Bioscience, Biotechnology, and Biochemistry
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Chiral Synthesis of the BC-Ring System of Ciguatoxin
from d-Glucose
Ei’ichi Amia, Hisakazu Kishimotoab, Hiroshi Ohruia & Hiroshi Meguroa
a Department of Applied Biological Chemistry, Faculty of Agriculture, Tohoku University,
Tsutsumidori-Amamiyamachi 1–1, Aobaku, Sendai 981, Japan
b Sumitomo Pharmaceutical Company, Kasugadenaka 3–1–98 Konohana-ku, Osaka 554,
Japan
Published online: 12 Jun 2014.
To cite this article: Ei’ichi Ami, Hisakazu Kishimoto, Hiroshi Ohrui & Hiroshi Meguro (1997) Chiral Synthesis of the BC-
Ring System of Ciguatoxin from d-Glucose, Bioscience, Biotechnology, and Biochemistry, 61:12, 2019-2024, DOI: 10.1271/
bbb.61.2019
To link to this article: http://dx.doi.org/10.1271/bbb.61.2019
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