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The reactions of mercurated pyrimidine nucleotides with thiols and with hydrogen sulfide.

In the presence of thiols, 5-mercuripyrimidine nucleotides are quantitatively converted to 5-thiomercuri derivatives, but these compounds are unstable and decompose at a rate dependent on the nature of the thiol. The decomposition involves three different reactions and proceeds via a symmetrical mer...

詳細記述

保存先:
書誌詳細
主要な著者: Van Broeckhoven, C, De Wachter, R
フォーマット: Artigo
言語:Inglês
出版事項: 1978
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC342149/
https://ncbi.nlm.nih.gov/pubmed/673847
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