Biomimetic systems involving sequential redox reactions in glycolysis - the sulfur effect
Narihito Ogawa1, Sei Furukawa2, Yuya Kosugi1
1Department of Applied Chemistry, Meiji University, Kawasaki, Kanagawa 214-8571, Japan. narihito@meiji.ac.jp.
Abstract:
Magnesium hemithioacetates were used as model cysteine compounds to mimic natural hemithioacetals, and their biomimetic oxidation reactions using a model NAD+ compound were investigated. Cyclic hemithioacetate was found to be the best substrate for the reaction with the model NAD+ compound, which gave the corresponding NADH analog in excellent yield.
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