1) α-phenylsulfonylcyclododecanone
α-苯磺酰基环十二酮
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。
2) 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。
3) acylaminocyclododecanone
α-酰氨基环十二酮
4) α-nitrocyclododecanone
α-硝基环十二酮
1.
Study on synthesis of α-nitrocyclododecanone;
α-硝基环十二酮的合成
2.
The structure of α-nitrocyclododecanone was confirmed by()~1H NMR and()~(13)C NMR.
以环十二烯为原料、NO2/O2为硝氧化试剂合成了α-硝基环十二酮。
3.
On this basis , 1 was synthesized by four-step two pot reaction sequence from α-nitrocyclododecanone in total yield of 77%.
以α-硝基环十二酮为原料合成12-氧代-1,15-十五内酯(1),文献报道有两种方法,即4步法和4步一锅法,后者的收率高于前者,对前者收率低的原因进行了研究,并在此基础上用4步两锅法以α-硝基环十二酮为原料合成了1,总收率77。
5) α-carbonylcyclododecanone
α-羰基环十二酮
1.
The keto-enol tautomerism of α-carbonylcyclododecanones has been studied by means of 1H NMR technology.
利用1H NMR技术研究了α-羰基环十二酮的酮-烯醇互变异构。
6) α-benzylcyclododecanone
α-苄基环十二酮
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。
补充资料:α-[2-(十二酰氨基)乙基]-&omega
CAS:26635-75-6
分子式:(C2H4O)nC14H29NO2
中文名称:聚乙二醇十二酰胺
α-[2-(十二酰氨基)乙基]-ω-羟基聚乙二醇
英文名称:2-ethanediyl), .alpha.-[2-[(1-oxododecyl)amino]ethyl]-.omega.-hydroxy-Poly(oxy-1 Lauric monoethanolamide, ethoxylate alpha-[2-[(1-oxododecyl)amino]ethyl]- omega -hydroxy-poly(oxy-2-ethanediyl) ethoxylated monoethanolamine of lauric
分子式:(C2H4O)nC14H29NO2
中文名称:聚乙二醇十二酰胺
α-[2-(十二酰氨基)乙基]-ω-羟基聚乙二醇
英文名称:2-ethanediyl), .alpha.-[2-[(1-oxododecyl)amino]ethyl]-.omega.-hydroxy-Poly(oxy-1 Lauric monoethanolamide, ethoxylate alpha-[2-[(1-oxododecyl)amino]ethyl]- omega -hydroxy-poly(oxy-2-ethanediyl) ethoxylated monoethanolamine of lauric
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