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・ 2.0 (Big Data album)
・ 2-Methoxyethyl-18-methoxycoronaridinate
・ 2-Methoxypropene
・ 2-Methyl-1-butanol
・ 2-Methyl-1-pentanol
・ 2-Methyl-2,4-pentanediol
・ 2-Methyl-2-butene
・ 2-Methyl-2-heptanethiol
・ 2-Methyl-2-nitrosopropane
・ 2-Methyl-2-pentanol
・ 2-Methyl-3-oxopropanoic acid
・ 2-Methyl-3-pentanol
・ 2-Methyl-3-phenylpiperidine
・ 2-Methyl-5-hydroxytryptamine
・ 2-Methyl-6-(phenylethynyl)pyridine
2-Methyl-6-nitrobenzoic anhydride
・ 2-methyl-branched-chain-enoyl-CoA reductase
・ 2-Methyl-MDA
・ 2-Methylacetoacetyl-CoA
・ 2-methylacetoacetyl-CoA thiolase
・ 2-methylacyl-CoA dehydrogenase
・ 2-Methylbutyryl-CoA
・ 2-Methylbutyryl-CoA dehydrogenase deficiency
・ 2-methylcitrate dehydratase
・ 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
・ 2-methylcitrate synthase
・ 2-methyleneglutarate mutase
・ 2-Methylfuran
・ 2-Methylheptane
・ 2-Methylhexane


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2-Methyl-6-nitrobenzoic anhydride : ウィキペディア英語版
2-Methyl-6-nitrobenzoic anhydride

2-Methyl-6-nitrobenzoic anhydride is a condensing agent also known as the Shiina reagent, having a structure wherein carboxylic acids undergo intermolecular dehydration condensation.
It was developed in 2002 by Prof. Isamu Shiina ''et al''. The compound is often abbreviated MNBA.
== Abstract ==
The reagent is used for synthetic reactions wherein medium- and large-sized lactones are formed from hydroxycarboxylic acids via intramolecular ring closure(Shiina macrolactonization). The reaction proceeds at room temperature under basic or neutral conditions. This reagent can be used not only for macrolactonization but also for esterification, amidation, and peptide coupling.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「2-Methyl-6-nitrobenzoic anhydride」の詳細全文を読む



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