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81.
New ruthenium(II) complexes carrying methionine and phenylalanine in the bipyridine ligand, [Ru(bpy)2(4-Me-4′-(CONH-l-methionine methyl ester)-2,2′-bipyridine)](PF6)2 (IV) and [Ru(bpy)2(4-Me-4′-(CONH-l-phenylalanine ethyl ester)-2,2′-bpy)](PF6)2(V) have been synthesized and characterized and their photophysical properties studied. Flash photolysis measurements of complex IV, in the presence of an electron acceptor, methyl viologen (MV2+) show that an intermolecular electron transfer from the excited state of Ru(II) in complex IV, to MV2+ takes place, forming Ru(III) and the methyl viologen cation radical, MV+. The formation of MV+ in this system is confirmed using time-resolved transient absorption spectroscopy. This intermolecular electron transfer is followed by intramolecular electron transfer from the thioether moiety (methionine) to the photogenerated Ru(III), regenerating Ru(II). 相似文献
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83.
M. Damodiran D. Muralidharan Paramasivan T. Perumal 《Bioorganic & medicinal chemistry letters》2009,19(13):3611-3614
The regioselective synthesis of 1,4-disubstituted 1,2,3-bistriazoles from a variety of N-propargyl bis(indolyl)methanes with sodium azide using CuI as the catalyst in polyethyleneglycol-400 is reported. This process is of considerable synthetic advantages in terms of high atom economy, low environmental impact, mild reaction condition and good yields. The synthesized compounds have also been screened for their biological activity. 相似文献
84.
Subramanian Vedhanarayanan Karthikeyan Subbu Perumal Krithika Arun Shetty Perumal Yogeeswari Dharmarajan Sriram 《Bioorganic & medicinal chemistry letters》2009,19(11):3006-3009
A series of novel 2-aryl-3,4-dihydro-2H-thieno[3,2-b]indoles has been synthesised regioselectively in good yields from the reaction of 5-aryldihydro-3(2H)-thiophenones and arylhydrazine hydrochloride. This reaction is found to be assisted by microwaves. The thieno[3,2-b]indoles were evaluated for their in vitro activity against Mycobacterium tuberculosis H37Rv (MTB) and multi-drug resistant M. tuberculosis (MDR-TB). Among 22 compounds screened, [2-(2,4-dichlorophenyl)-7-fluoro-3,4-dihydro-2H-thieno[3,2-b]indole] (6t) was found to the most active compound with MIC of 0.4 μg/mL against MTB and MDR-TB. 相似文献
85.
Dharmarajan Sriram Perumal Yogeeswari Prathiba Dhakla Palaniappan Senthilkumar Debjani Banerjee Thimmappa H. Manjashetty 《Bioorganic & medicinal chemistry letters》2009,19(4):1152-1154
Eighteen 5-nitrofuran-2-yl derivatives were prepared by reacting 5-nitro-2-furfural with various (sub)phenyl/pyridyl thiosemicarbazide using microwave irradiation. The compounds were tested for their in vitro activity against tubercular and various non-tubercular mycobacterium species in log-phase and 6-week-starved cultures. Compound N-(3,5-dibromopyridin-2-yl)-2-((5-nitrofuran-2-yl)methylene)hydrazinecarbothioamide (4r) was found to be the most potent compound (MIC: 0.22 μM) and was 3 times more active than standard isoniazid (INH) and equally active as rifampicin (RIF) in log-phase culture of Mycobacterium tuberculosis H37Rv. In starved M. tuberculosis H37Rv, 4r inhibited with MIC of 13.9 μM and was found to be 50 times more active than INH and slightly more active than RIF. 相似文献
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88.
Rajakumar P Mohammed Abdul Rasheed A Iman Rabia A Chamundeeswari D 《Bioorganic & medicinal chemistry letters》2006,16(23):6019-6023
Macrocyclic di- and tetra-amides with thia- and oxylinkages were synthesized and screened for in vitro anti-inflammatory activity. Cyclophane diamide 15 showed a dose-dependent activity, while the other cyclophane amides 16-20 exhibited mild activity. 相似文献
89.
Sivaprasad G Perumal PT Prabavathy VR Mathivanan N 《Bioorganic & medicinal chemistry letters》2006,16(24):6302-6305
A series of pyrazolylbisindole derivatives have been synthesized by reacting substituted pyrazole aldehydes with substituted indoles using phosphotungstic acid, a Keggin type heteropoly acid as catalyst. The synthesized pyrazolylbisindoles were evaluated for anti-microbial activities. The effect of pyrazolylbisindoles on the mycelial growth of plant pathogenic fungi is revealed. Entries 3c and 3d emerged as the most interesting compounds in this series exhibiting excellent anti-fungal activity. 相似文献
90.
Venkatachalam SR Salaskar A Chattopadhyay A Barik A Mishra B Gangabhagirathi R Priyadarsini KI 《Bioorganic & medicinal chemistry》2006,14(18):6414-6419
A novel conjugate of melatonin 2 and alpha-lipoic acid 4 has been prepared using DCC mediated coupling. The conjugate named melatoninolipoamide has been assigned its structure 1 on the basis of spectral analysis (UV, IR, NMR, and EI-MS). Pulse radiolysis studies of the conjugate were carried out in aqueous solutions with both oxidizing and reducing radicals. The results indicate that the melatonin moiety of the conjugate reacts preferably with oxidizing radicals and the lipoic acid moiety exhibits preferential reaction with reducing radicals. The in vitro radioprotection ability of 1 was examined by gamma-radiation induced lipid peroxidation in liposomes and hemolysis of erythrocytes, and compared the results with those of melatonin and alpha-lipoic acid. The studies suggest that the conjugate can be explored as a probable radioprotector. 相似文献