5篇
您的检索式：作者名="ABLAJAN Keyume"
|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | The convenient synthesis of 4-arylmethylidene-4,5-dihydro-3-phenylisoxazol-5-ones显示文摘4-Arylmethylidene-4,5-dihydro-3-phenylisoxazol-5-ones 被乙醇 benzoylacetate, hydroxylamine 和芳香的醛的方便三部件的反应面对 pyridine 综合。目标混合物被在 3-phenylisoxazol-5-one 和芳香的醛之间的反应也在 105 | Keyume Ablajan Hainimu Xiamuxi | 2011 | Chinese Chemical Letters2011，22，2： | 2 |
| 2 | Cetyltrimethylammonium chloride(CTAC)catalyzed one-pot synthesis of novel coumarin-4H-pyran conjugates in aqueous media显示文摘Novel fluorescent coumarin-4H-pyran conjugates were achieved by three-component reactions of various synthetic β-ketoesters with aldehydes and malononitrile in aqueous media.Besides mild reaction conditions,operational simplicity,absence of tedious separation procedures,using of inexpensive and nontoxic commercially available cationic surfactant cetyltrimethylammonium chloride(CTAC) as a catalyst are the prominent advantage of this method. | Adil Omar Keyume Ablajan Mawjvda Hamdulla | 2017 | Chinese Chemical Letters2017，28，5： | 2 |
| 3 | Structural characterization of flavonol 3,7-di-O-glycosides and determination of the glycosylation position by using negative ion electrospray i- onization tandem mass spectrometry 显示文摘 | Keyume Ablajan Zeper Abliz Xiao-Ya Shang | 2006 | J Mass Speetrom2006，41，： | 1 |
| 4 | Seasonal variations in metabolite profiling of the fruits of Ligustrum lucidum Ait 显示文摘 | Guo Na Yu Youhua Ablajan Keyume | 2011 | Rapid Commu Mass Spectrum2011，25，12： | 1 |
| 5 | Furans-Maleimides Diels-Alder Reactions in Protic Ionic Liquid显示文摘The authors have studied the Diels-Alder reactions between furan derivatives and maleimide derivatives in an ionic liquid and have found that higher reactivity can be obtained in a protic ionic liquid [Mim]Tf2N than in the conventional organic solvent. Furthermore, in the Diels-Alder reactions of 2- and 2,5-alkylfurans with N-alkylma-leimide, the reactivity increases by extending the alkyl chain length of N-alkylmaleimide. In addition, it was demon-strated that endo-selectivity increases when 2,5-disubstituted furans are used. These results will be explained by comparing the stability of the Diels-Alder adduct with that of the products obtained from the reactions of 2-substituted furans and 2,5-disubstituted furans. | XAWKAT Ahmat ABLAJAN Keyume HIRAKU Shinozaki | 2009 | Chemical Research in Chinese Universities2009，25，2： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员