翻訳と辞書 Words near each other ・ 1-Nitropyrene ・ 1-Nonacosanol ・ 1-Nonanol ・ 1-Nonyl-4-phenol ・ 1-Nonylnaphthalene ・ 1-NP ・ 1-Octacosanol ・ 1-Octanol ・ 1-Octen-3-ol ・ 1-Octen-3-yl acetate ・ 1-Octene ・ 1-OQA+19 ・ 1-Page ・ 1-Pentanol ・ 1-Pentyne ・ 1-Phenylethylamine ・ 1-phosphatidylinositol 4-kinase ・ 1-phosphatidylinositol-3-phosphate 5-kinase ・ 1-phosphatidylinositol-4-phosphate 5-kinase ・ 1-phosphatidylinositol-5-phosphate 4-kinase ・ 1-phosphofructokinase ・ 1-planar graph ・ 1-Propanol ・ 1-Pyrroline dehydrogenase ・ 1-pyrroline-4-hydroxy-2-carboxylate deaminase ・ 1-Pyrroline-5-carboxylate dehydrogenase ・ 1-Pyrroline-5-carboxylic acid ・ 1-Testosterone ・ 1-Tetracosanol ・ 1-Tetradecanol Dictionary Lists mini英和辞書 mini和英辞書 Webster 1913 Latin-English FOLDOC Wikipedia English ウィキペディア

翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク 1-Phenylethylamine ： ウィキペディア英語版 | Section2 = | Section7 = | Section8 = }}1-Phenylethylamine is a monoamine compound. Individual enantiomers of this basic compound are useful for performing chiral resolution of acidic compounds by forming diastereomeric salts and for performing chiral hydrogenations of ketones resulting in enantiopure amines.This compound may be prepared by the reductive amination of acetophenone under various standard conditions for this type of reaction. One major route for this chemical uses the Mignonac reaction,reductive amination, but could some day have its own page forked from it --> a one-pot protocol using hydrogen gas as the reducing agent: :The Leuckart reaction, using ammonium formate, is another method for this transformation.== See also ==* 2-Phenylethylamine | Section2 = | Section7 = | Section8 = }} 1-Phenylethylamine is a monoamine compound. Individual enantiomers of this basic compound are useful for performing chiral resolution of acidic compounds by forming diastereomeric salts and for performing chiral hydrogenations of ketones resulting in enantiopure amines. This compound may be prepared by the reductive amination of acetophenone under various standard conditions for this type of reaction. One major route for this chemical uses the Mignonac reaction, a one-pot protocol using hydrogen gas as the reducing agent: : The Leuckart reaction, using ammonium formate, is another method for this transformation. == See also == * 2-Phenylethylamine 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「| Section2 = | Section7 = | Section8 = }}1-Phenylethylamine is a monoamine compound. Individual enantiomers of this basic compound are useful for performing chiral resolution of acidic compounds by forming diastereomeric salts and for performing chiral hydrogenations of ketones resulting in enantiopure amines.This compound may be prepared by the reductive amination of acetophenone under various standard conditions for this type of reaction. One major route for this chemical uses the Mignonac reaction,reductive amination, but could some day have its own page forked from it --> a one-pot protocol using hydrogen gas as the reducing agent: :The Leuckart reaction, using ammonium formate, is another method for this transformation.== See also ==* 2-Phenylethylamine」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.