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・ Alkylglycerol monooxygenase
・ Alkylglycerone kinase
・ Alkylglycerone phosphate synthase
・ Alkylglycerophosphate 2-O-acetyltransferase
・ Alkylglycerophosphoethanolamine phosphodiesterase
・ Alkylhalidase
・ Alkylimino-de-oxo-bisubstitution
・ Alkylmercury lyase
・ Alkylphenol
・ Alkylphosphocholine
・ Alkylpyrazine
・ Alkylresorcinol
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・ Alkyne trimerisation
Alkyne zipper reaction
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Alkyne zipper reaction : ウィキペディア英語版
Alkyne zipper reaction
The alkyne zipper reaction is an organic reaction which isomerizes an organic compound containing an internal alkyne into a terminal alkyne. This was first reported by Charles Allen Brown and Ayako Yamashita in 1975. The isomerization reaction proceeds for straight-chain alkynes and acetylinic alcohols and provides a useful approach for remote functionalization in long-chain hydrocarbons.〔
The reaction requires a strong base. The base used by Brown and Yamashita was potassium 1,3-diaminopropanide, generated ''in situ'' by adding potassium hydride to the solvent 1,3-diaminopropane.〔 Alternative approaches have been investigated due to the expensive and hazardous nature of potassium hydride; ethylenediamine has been found to be an unsuitable replacement for 1,3-diaminopropane. As an example, for the synthesis of 9-decyn-1-ol from 2-decyn-1-ol, the lithium salt of 1,3-diaminopropane in the presence of potassium ''tert''-butoxide affords yields of approximately 85%.
:HO–CH2C≡C–(CH2)6CH3 → HO(CH2)8–C≡CH
==References==


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