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・ Acyl-homoserine-lactone synthase
・ Acyl-lysine deacylase
・ Acyl-phosphate—hexose phosphotransferase
・ Acylagmatine amidase
・ Acylal
・ Acylaminoacyl-peptidase
・ Acylase
・ Acylation
・ Acylation stimulating protein
・ Acylcarnitine hydrolase
・ Acyldepsipeptide antibiotics
・ Acylfulvene
・ Acylglycerol kinase
・ Acylglycerol lipase
・ Acylglycerone-phosphate reductase
Acylhydrazine
・ Acylita
・ Acylita cara
・ Acylita distincta
・ Acylita dukinfieldi
・ Acylita elongata
・ Acylita monosticta
・ Acylita sanguifusa
・ Acyloin
・ Acyloin condensation
・ Acyloxyacyl hydrolase
・ Acylphosphatase
・ Acylpyruvate hydrolase
・ Acylsilane
・ Acylsugar


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Acylhydrazine : ウィキペディア英語版
Acylhydrazine

An acylhydrazine is analogous to an amide, but the -OH portion of a carboxylic acid is replaced by hydrazine rather than ammonia (one less hydrogen at the point of attachment). Acylhydrazines are a type of hydrazides.
Acylhydrazines are intermediates in chemical syntheses. For example, a synthesis of sunitinib begins by mixing 5-fluoroisatin slowly into hydrazine hydrate. After 4 hours at 110 °C, the indole ring structure has been broken into (2-amino-5-fluoro-phenyl)-acetic acid hydrazide with reduction of the ketone at the 3-position. Subsequent annelation in strong acid creates the 1,3-dihydro-2-oxo indole structure required for the drug.
== References ==



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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