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・ 2-Mercaptoethanol
・ 2-Mercaptoindole
・ 2-Mercaptopyridine
・ 2-meter band
・ 2-Methoxy-4-vinylphenol
・ 2-Methoxy-6-polyprenyl-1,4-benzoquinol methylase
・ 2-Methoxyamphetamine
・ 2-Methoxyestradiol
・ 2-Methoxyethanol
・ 2-Butoxyethanol acetate
・ 2-Butyne
・ 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase
・ 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase
・ 2-C-Methyl-D-erythritol-2,4-cyclopyrophosphate
・ 2-C-Methylerythritol 4-phosphate
2-Carbomethoxytropinone
・ 2-Carboxy-D-arabinitol-1-phosphatase
・ 2-category
・ 2-chloro-4-carboxymethylenebut-2-en-1,4-olide isomerase
・ 2-Chloro-9,10-bis(phenylethynyl)anthracene
・ 2-Chloro-9,10-diphenylanthracene
・ 2-Chloro-m-cresol
・ 2-chlorobenzoate 1,2-dioxygenase
・ 2-Chlorobenzoic acid
・ 2-Chlorobutane
・ 2-Chloroethanesulfonyl chloride
・ 2-Chloroethanol
・ 2-Chlorophenol
・ 2-Chloropropionic acid
・ 2-Chloropyridine


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2-Carbomethoxytropinone : ウィキペディア英語版
2-Carbomethoxytropinone

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2-Carbomethoxytropinone (2-CMT) is a commonly used organic intermediate in the synthesis of cocaine and its analogues. As of at least 1999 no reaction pathway has been discovered that synthesizes cocaine-like compounds without utilizing the reduction of 2-carbomethoxytropinone. The structure of cocaine was discovered by Richard Willstätter in 1898 after he synthesized it from 2-carbomethoxytropinone. Although it was originally believed that 2-CMT in nature was ultimately derived from ornithine and acetic acid, subsequent research has indicated other pathways exist for the biosynthesis of 2-CMT. A β-keto ester, 2-carbomethoxytropinone exists in equilibrium with its keto–enol tautomer.
==Synthesis==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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