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Biomimetic systems involving sequential redox reactions in glycolysis – the sulfur effect†
Narihito Ogawa,Sei Furukawa,Yuya Kosugi,Takayuki Takazawa,Nobuhiro Kanomata
Chemical Communications Pub Date : 09/25/2020 00:00:00 , DOI:10.1039/D0CC05185C
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.

Graphical abstract: Biomimetic systems involving sequential redox reactions in glycolysis – the sulfur effect
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