Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me<sub>2</sub>NS0<sub>2</sub>Cl and N,N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide

WAKASUGI K; NAKAMURA A; IIDA A; NISHII Y; NAKATANI N; FUKUSHIMA S; TANABE Y

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J-GLOBAL ID：200902297689568208 Reference number：03A0511854

Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me₂NS0₂Cl and N,N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide

Me₂NSO₂Cl及びN,N-ジメチルアミン類を利用するカルボン酸と等モル量のアルコール及びアミンとの間のエステル化,アミド化のための新しい効率的な方法天然化学予防剤ジエンアミドのクマペリンの合成に対するその適用

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Material：
Volume： 59 Issue： 28 Page： 5337-5345 Publication year： Jul. 07, 2003
JST Material Number： E0234A ISSN： 0040-4020 Document type： Article
Article type：原著論文 Country of issue： United Kingdom (GBR) Language： ENGLISH (EN)

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Aliphatic sulfonic acid,sulfinic acid,sulfenic acid and other compounds , Addition reaction,elimination reaction

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Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me2NS02Cl and N,N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide

Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me₂NS0₂Cl and N,N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide