1) aroylamino
芳酰氨基
1.
Synthesis and Biological Activities of 2-aroylamino-5-(4-pyridyl)-1,3,4-thiadiazoles;
5-(4-吡啶基)-2-芳酰氨基-1,3,4-噻二唑的合成及生物活性
2.
Synthesis and biological activity of 2-aroylamino-5-pyridyl-1,3,4-thiadiazoles;
5-吡啶基-2-芳酰氨基-1,3,4-噻二唑的合成及生物活性
3.
Five derivatives of 2-aroylamino-5-(pyrid-3-yl)1,3,4-thiadiazoles IIIa~e have been synthesized by amidation of 2-amino-5-(pyrid-3-yl)-1,3,4-thiadiazoles and substituted benzoyl chloride.
利用2-氨基-5-(3-吡啶基)-1,3,4-噻二唑和取代苯甲酰氯的酰化反应,合成了5个5-(3-吡啶基)-2-芳酰氨基-1,3,4-噻二唑类化合物Ⅲa~e,其结构经1H NMR、IR和元素分析方法证实。
2) aroylthiosemicarbazide
芳酰基氨基硫脲
1.
1-[(2-Trifluoromethylbenzimidazol-1-yl)acetyl]-4-aroylthiosemicarbazide derivatives 1a～1j were synthesized by the reaction of 1-hydrazinocarbonylmethyl-2-trifluoromethylbenzoimidazole with aroylisothiocyanate under microwave irradiation.
微波辐射下,1-肼羰亚甲基-2-三氟甲基苯并咪唑与芳酰基异硫氰酸酯反应合成了1-(2-三氟甲基苯并咪唑-1-乙酰基)-4-芳酰基氨基硫脲(1a～1j),继而在乙酸中合环得到了一系列的2-芳甲酰氨基-5-(2-三氟甲基苯并咪唑-1-亚甲基)-1,3,4-噻二唑(2a～2j),反应时间短,产率高,副反应少。
3) arylglycine amide
芳基甘氨酰胺
1.
Enantiomers of nine arylglycine amides synthesized were successfully separated by capillary electrophoresis (CE) using highly sulfated β cyclodextrin (HS β CD) as a chiral selector.
研究了 9种自行合成的芳基甘氨酰胺的手性拆分。
4) aroylthiosemicarbazides
芳酰氨基硫脲
1.
Synthesis and Study on the 1-pyridinoyl-4-aroylthiosemicarbazides;
1-(3-吡啶甲酰基)-4-芳酰氨基硫脲类化合物的合成
5) N-aroylglycine
N-芳酰基甘氨酸
1.
We found that using ammonium persulfate as a oxidant and water/CHCl3 as solvents, N-aroylglycine underwent oxidative decarboxylation to afford N-formylbenzamides at 60°C.
本论文对N-芳酰基甘氨酸在银催化下的氧化脱羧反应进行了研究。
6) 1-arylaminoacetyl-4-arylacetyl thiosemicarbazide
1-芳氨基乙酰基-4-芳乙酰基氨基硫脲
补充资料：氨基酰合成酶或氨基酰-tRNA合成酶
氨基酰合成酶或氨基酰-tRNA合成酶
催化一个特定氨基酸与ATP形成AA-AMP，并使AA-AMP与特定的tRNA相结合形成AA-tRNA和游离AMP的酶，已发现20余种。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条