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1)  α-methylthiocyclododecanone oxime ester
α-甲硫基环十二酮肟酯
1.
Sixteen new α-methylthiocyclododecanone oxime esters were synthesized by the reaction of acylation of α-methylthiocyclododecanone oxime as intermediate with acids.
以环十二酮为原料,经α-甲硫基环十二酮肟合成了16个新的α-甲硫基环十二酮肟酯,其结构经元素分析1、H NMR1、3C NMR和IR的确证。
2)  α-methylthiocyclododecanone oxime ether
α-甲硫基环十二酮肟醚
1.
Ten new α-methylthiocyclododecanone oxime ether were synthesized by the (reaction) of (alkylation) of α-methylthiocyclododecanone oxime as intermediate with alkyl halides, which were (prepared) from α-methylthiocyclododecanone oxime and cyclododecanone as starting material.
以环十二酮为原料,经α-甲硫基环十二酮制得中间体α-甲硫基环十二酮肟后,经烷基(芳基)化反应合成了10个α-甲硫基环十二酮肟醚,其结构经元素分析1、H NMR1、3C NMR和IR的确证。
3)  α-benzylcyclododecanone oxime ester
α-苄基环十二酮肟酯
1.
Twenty-two novel compounds of α-benzylcyclododecanone oxime esters were synthesized by the acylation of α-benzylcyclododecanone oxime.
以环十二酮为原料,经过α-取代反应生成中间体α-苄基环十二酮,再与羟胺作用成肟,再经酯化反应合成了22个未见文献报道的α-苄基环十二酮肟酯衍生物,其化学结构经1H NMR、IR和元素分析确证。
4)  α-methylthiocyclododecanone
α-甲硫基环十二酮
1.
Sixteen new α-methylthiocyclododecanone oxime esters were synthesized by the reaction of acylation of α-methylthiocyclododecanone oxime as intermediate with acids.
以环十二酮为原料,经α-甲硫基环十二酮肟合成了16个新的α-甲硫基环十二酮肟酯,其结构经元素分析1、H NMR1、3C NMR和IR的确证。
2.
Ten new α-methylthiocyclododecanone oxime ether were synthesized by the (reaction) of (alkylation) of α-methylthiocyclododecanone oxime as intermediate with alkyl halides, which were (prepared) from α-methylthiocyclododecanone oxime and cyclododecanone as starting material.
以环十二酮为原料,经α-甲硫基环十二酮制得中间体α-甲硫基环十二酮肟后,经烷基(芳基)化反应合成了10个α-甲硫基环十二酮肟醚,其结构经元素分析1、H NMR1、3C NMR和IR的确证。
5)  α-phenylsulfonylcyclododecanone oxime ester
α-苯磺酰基环十二酮肟酯
1.
Twenty novel compounds of α-phenylsulfonylcyclododecanone oxime esters (8) were synthesized by the acylation of α-phenylsulfonylcyclododecanone oxime.
以环十二酮为原料,经过α-取代反应生成中间体α-苯磺酰基环十二酮,先与NH2OH作用成肟然后酯化反应合成了20个未见文献报道的α-苯磺酰基环十二酮肟酯衍生物(8),其化学结构经1HNMR,IR和元素分析确证。
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6)  α-monosubstituted cyclododecanone oxime
α-单取代环十二酮肟
1.
Two kinds of α-monosubstituted cyclododecanone oximes and thiosemicarbazones were synthe-sized by the reaction of α-monosubstituted cyclododecanone with hydroxylamine and 4-p-tolylthiosemicar-bazide.
单晶X射线衍射分析表明,α-单取代环十二酮与氨衍生物羟胺和氨基硫脲发生缩合反应得到两种母体构象均为[3333],而取代基为边外向或角反向的α-单取代环十二酮肟或缩氨基硫脲。
补充资料：甲硫基乙醛肟
分子式：C3H7NOS
分子量：105.1544
CAS号：暂无

性质：暂无

制备方法：暂无

用途：暂无

说明：补充资料仅用于学习参考，请勿用于其它任何用途。
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