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・ N-malonylurea hydrolase
・ N-methyl nucleosidase
・ N-methyl-2-oxoglutaramate hydrolase
・ N-Methyl-2-pyrrolidone
・ N-Methyl-3-piperidyl benzilate
・ N-Methyl-D-aspartic acid
・ N-methyl-L-amino-acid oxidase
・ N-Methyl-L-glutamic acid
・ N-Methyl-N-ethyltryptamine
・ N-Methyl-PPPA
・ N-methylalanine dehydrogenase
・ N-Methylaniline
・ N-Methylcarfentanil
・ N-methylcoclaurine 3'-monooxygenase
・ N-Methylconiine
N-Methylephedrine
・ N-Methylethanolamine
・ N-Methylformamide
・ N-methylhydantoinase (ATP-hydrolysing)
・ N-Methylhydroxylamine
・ N-Methylmaleimide
・ N-Methylmescaline
・ N-Methylmorpholine
・ N-Methylmorpholine N-oxide
・ N-Methylornithine
・ N-Methylphenethylamine
・ N-methylphosphoethanolamine cytidylyltransferase
・ N-Methylpseudoephedrine
・ N-Methylserotonin
・ N-Methylspiperone


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N-Methylephedrine : ウィキペディア英語版
N-Methylephedrine

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''N''-Methylephedrine is a derivative of ephedrine. It has been isolated from ''Ephedra distachya''.
In organic chemistry, ''N''-methylephedrine is used as a resolving agent and as a precursor to chiral supporting electrolytes, phase-transfer catalysts, and reducing agents.〔((1R,2S)-(−)-N-Methylephedrine ) at Sigma-Aldrich
==See also==

* ''N''-Methylpseudoephedrine

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「N-Methylephedrine」の詳細全文を読む



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