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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

O-Ethyl-L-homoserine synthesis

3synthesis methods
Homoserine, O-ethyl-

17804-70-5
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O-Ethyl-L-homoserine

17268-93-8
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-

Yield:-

Steps:

Multi-step reaction with 3 steps
1: aq. NaOH / dioxane
2: aq. KCN / (microbiological transformation)
3: aq. HCl

References:

Murooka;Harada;Izumi [Bulletin of the Chemical Society of Japan,1968,vol. 41,# 3,p. 633 - 635]

L-Homoserine, O-ethyl-N-(triphenylmethyl)-

85918-07-6
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O-Ethyl-L-homoserine

17268-93-8
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References
Homoserine, O-ethyl-N-[(phenylmethoxy)carbonyl]-

18634-96-3
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O-Ethyl-L-homoserine

17268-93-8
3 suppliers
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References