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1.
Here, we report a new strategy for rapid synthesis of branched peptide by side-chain hydrazide ligation at Asn. The hydrazide was converted to thioester at Asn side chain by NaNO2 and thiol reagent, and sequential ligation with an N-terminus Cys-peptide efficiently afforded the branched peptide. A branched cyclic peptide was successfully synthesized by side-chain ligation with a two-Cys-peptide and formation of a disulfide bond. This approach provides a new way for expeditious synthesis of branched peptides and facilitates the design of neopeptides as functional bio-mimics. 相似文献
2.
Ming Zhao WANG Guan Liang CAI Ling XIA Jun Jian YAO Hong Yan CHEN Zhao Xing MENG Bo Li LIUDepartment of Chemistry Beijing Normal University Beijing Chemical Defense Institute PLA Beijing 《中国化学快报》2004,15(4):495-497
The crystal structures of two potential tumor imaging agents and therapeutic agents -copper(Ⅱ) complexes with salicylidene-tyrosinato Schiff base and nitrogen-donor chelating Lewis base, [Cu(sal-tyr)(bipy)] 1 and [Cu(sal-tyr)(phen)]2CH3OH 2 are presented. Our work is helpful to get deep understanding of novel 64Cu tumor imaging agents and therapeutic agents. 相似文献
3.
4.
The Rubiaceae family is well known for containing anthraquinones. More specifically, lapachol and its analogues are known to possess antitumor, antibiotic, antimalarial and antiulceric activities.[1] Several report indicated that some quinones containing OH in its structure were found to have higher bio-activity than quinines lacking the OH group. 相似文献
5.
StudiesonthePlasmaShieldingof1.06μmLaserontheAluminumTargetLUJian;NIXiaowu;HEAnzhi(DepartmentofAppliedPhysics,NanjingofScienc... 相似文献
6.
Xin Ying ZHANG Xue Sen FAN Hong Ying NIU Jian Ji WANGSchool of Chemical Environmental Sciences Henan Normal University Key Laboratory ofEnvironmental Science Engineering of Henan Education Department Xinxiang 《中国化学快报》2003,(10)
a, a'-Bis(substituted benzylidene)cycloalkanones were efficiently prepared from cycloalkanones and benzaldehydes in [bmim][BF4] by using iron(III) chloride hexahydrate as a catalyst. It is shown that [bmim][BF4] and iron(III) chloride hexahydrate can be quantitatively recovered and be reused effectively for many times. Compared with the known methods, this novel process has the advantage of being an envkonmentally benign process together with good yields and mild reaction conditions. 相似文献
7.
Yong-liang Zhu Bin Wang Jian Yu Zhao-xia Guo 《高分子科学》2007,(3):291-296
PEG (Polyethylene Glycol)-grafted nano-titania has been obtained in a one-step procedure using hexamethylene diisocyanate as the coupling agent and dibutyltin dilaurate as the catalyst in toluene at 80℃ and characterized qualitatively by FTIR and quantitatively by elemental analysis and thermogravimetric analysis. A comparison of nano-titania with two other commonly used inorganic nanoparticles, nano-silica and nano-alumina, is made, revealing that reactivity order is nano- silica 〉 nano-alumina 〉 nano-titania in view of PEG grafting. Possible mechanism of PEG grafting is also discussed. 相似文献
8.
Fa Jie Yang Da Ling Yang Shou Hai Zhang Xi Gao Jian 《中国化学快报》2007,18(8):966-968
A new interfacial polymerization (IP) procedure is developed in order to synthesize polypiperazine-amide thin-film membrane on the inner surface of poly(phthalazinone ether sulfone ketone) (PPESK) hollow fiber ultrafiltration (UF) membrane.A hollow fiber composite membrane with good performance was prepared and studied by FT-IR and scanning electron microscopy. 相似文献
9.
Ye Qing Li Ming Lu Chun Xu Lu Sai Jian Zhu Qi Fa Liu 《中国化学快报》2007,18(11):1313-1315
A novel and simple procedure for synthesis of azanucleoside by Mitsunobu reaction between N-(p-nitrobenzyloxycarbonyl)- trans-4-hydroxy-D-proline methyl ester obtained from trans-4-hydroxy-L-proline after six-step reaction and 2-fluoro-6-azidopurine is described,and azanucleoside is fluorinated by new fluridizer 2,2-difluoro-1,3-dimethylimidazolidine (DFI).All reactions could be carded out under mild condition. 相似文献
10.
1-substituted-5-benzoylamino-4-pyrazolecarboxamides(2)were prepared by the reaction of 1-substituted pyrazolo[3, 4-d]-oxazinone(1)with amines in benzene.The compound 2 was refluxed with excess LiAlH4 in a mixture of THF and ether, one of the two carbamoyl groups in the molecule 2 was reduced selectively.As the results, 1-substituted-5-benzylamino-4-pyrazolecarboxamides (3) were obtained.Compounds 3reacted with Cl2PPh-X, or P(NET2)3, producing the title compounds(4).The conditions of the reactions were studied. 相似文献