全文获取类型
收费全文 | 4125篇 |
免费 | 99篇 |
国内免费 | 21篇 |
专业分类
化学 | 2918篇 |
晶体学 | 46篇 |
力学 | 48篇 |
数学 | 182篇 |
物理学 | 1051篇 |
出版年
2022年 | 17篇 |
2021年 | 34篇 |
2020年 | 45篇 |
2019年 | 54篇 |
2018年 | 43篇 |
2017年 | 23篇 |
2016年 | 56篇 |
2015年 | 74篇 |
2014年 | 67篇 |
2013年 | 177篇 |
2012年 | 177篇 |
2011年 | 236篇 |
2010年 | 108篇 |
2009年 | 140篇 |
2008年 | 220篇 |
2007年 | 227篇 |
2006年 | 238篇 |
2005年 | 192篇 |
2004年 | 182篇 |
2003年 | 169篇 |
2002年 | 178篇 |
2001年 | 131篇 |
2000年 | 107篇 |
1999年 | 70篇 |
1998年 | 52篇 |
1997年 | 57篇 |
1996年 | 55篇 |
1995年 | 41篇 |
1994年 | 56篇 |
1993年 | 64篇 |
1992年 | 77篇 |
1991年 | 59篇 |
1990年 | 50篇 |
1989年 | 60篇 |
1988年 | 45篇 |
1987年 | 57篇 |
1986年 | 47篇 |
1985年 | 57篇 |
1984年 | 52篇 |
1983年 | 41篇 |
1982年 | 29篇 |
1981年 | 42篇 |
1980年 | 32篇 |
1979年 | 51篇 |
1978年 | 41篇 |
1977年 | 26篇 |
1976年 | 32篇 |
1975年 | 26篇 |
1974年 | 30篇 |
1973年 | 21篇 |
排序方式: 共有4245条查询结果,搜索用时 546 毫秒
111.
Angiotensin I‐converting enzyme (ACE) inhibitory peptide was isolated from the hen ovotransferrin hydrolysate using chymotryptic hydrolysis by two steps of reverse‐phase high‐performance liquid chromatography. The amino sequence of this novel peptide was identified as Lys‐Val‐Arg‐Glu‐Gly‐Thr‐Thr‐Tyr that inhibited ACE activity in vitro in a concentration‐dependent manner with an effective concentration (IC50) of 102.8 μM. Also, this inhibition was identified as noncompetitive using the Lineweaver‐Burk plot. Moreover, the antihypertensive action of this novel peptide was investigated by an intravenous injection into spontaneously hypertensive rats (SHR). A dose‐dependent reduction of systolic blood pressure by this peptide was observed after 40 min of treatment and it decreased the blood pressure markedly at the maximal dose (1 nmol/mL/kg). The maximal blood pressure lowering activity of this peptide was calculated as 163% of captopril (10 pmol/mL/kg) that was used as positive control. In conclusion, the obtained data suggests that Lys‐Val‐Arg‐Glu‐Gly‐Thr‐Thr‐Tyr has an ability to inhibit ACE activity and decrease the systolic blood pressure in hypertensive animals. 相似文献
112.
The three-component aminoallylation reaction of the activated olefins 2 with the phthalimide 1a and allyl chloride proceeded very smoothly in the presence of Pd(2)dba(3).CHCl(3) (5 mol %)/P(4-FC(6)H(4))(3) (40 mol %) and Cs(2)CO(3) (3 equiv against 2) in dichloromethane at room temperature to give the corresponding aminoallylated products, N-pent-4-enylphthalimides 3, in 58-99% yields. The reaction of oxazolidinone 1b also proceeded very smoothly to give N-(2,2-dicyano-1-phenylpent-4-enyl)oxazolidinone in a quantitative yield; however, the Tsuji-Trost-type allylation products 4 were obtained in the case of dibenzylamine, N-tosylaniline, and pyrrolidin-2-one. Further, 2 underwent cycloaddition with N-tosylvinylaziridine 9a in the presence of Pd(2)dba(3).CHCl(3) (5 mol %)/P(4-FC(6)H(4))(3) (40 mol %) in THF at room temperature, giving the corresponding pyrrolidines 11 in 69-99% yields. 相似文献
113.
Yoshiki Chujo Tetsuya Nakamura Yuya Yamashita 《Journal of polymer science. Part A, Polymer chemistry》1990,28(1):59-65
Mercapto-16-crown-5 was prepared starting from tetraethyleneglycol and 3-chloro-2-chloromethyl-1-propene. Radical polymerization of methyl methacrylate was carried out in the presence of mercapto-16-crown-5 as a chain transfer agent to give crown ether-terminated poly(methyl methacrylate). The end crown group was characterized by IR and 1H-NMR spectra. Sodium cation was selectively extracted by this crown-containing polymer. The molecular weight of the obtained polymer had influence upon the ability of extraction of sodium cation. 相似文献
114.
Base-catalyzed reaction of 5-acylmethyl-2,5-di--butyl-4-oxa-2-cyclopentenones selectively derived from 4-alkyl-2,6-di--butylphenols three steps involving oxygenation, acetylation, and acid-treatment gave 3-alkyl-2,5-di--butyl-2,4-cyclopentadienones in excellent yield. 相似文献
115.
Phenols are deprotected with weak bases from their tert-butoxycarbonyl (Boc) derivatives. Boc deprotection with bases can avoid side reactions during the deprotection with acids. We note the lability of the Boc to bases and are able to utilize it as a new cleavage condition for synthetic studies. 相似文献
116.
Ishimitsu S Kaihara A Yoshii K Tsumura Y Nakamura Y Tonogai Y 《Journal of AOAC International》2001,84(4):1172-1178
A method was developed for determination of the herbicide clethodim (C0) and its oxidation metabolites clethodim sulfoxide (C1) and clethodim sulfone (C2) in agricultural products. Upon extraction, both C0 and C1 were oxidized to C2 by m-chloroperoxybenzoic acid, and C2 was determined by liquid chromatography (LC). The C2 peak was confirmed by liquid chromatography/mass spectrometry (LC/MS) with electrospray ionization (ESI). Recoveries of C0 from radish, tomato, onion, sweet potato, kidney bean, carrot, cabbage, and lettuce ranged from 91 to 118% following fortification at 0.05-1.0 ppm. The detection limit of C2 in crops was 0.01 ppm (S/N > 3). The fortified samples of onion, sweet potato, kidney bean, and carrot were confirmed by LC/MS (ESI), and the peak of C2 was detected. 相似文献
117.
118.
3-Epi-6,7-dideoxyxestobergsterol A (2), an analogue of xestobergsterol A, has been synthesized from dehydroepiandrosterone (3) in 15 steps. The key synthetic intermediate, 15beta,16alpha-dioxypregn-17(20)E-ene derivative 8, was prepared from the corresponding 15beta,16beta-epoxide 6 by treating with acetic acid and titanium tetraisopropoxide. The 23-oxo side chain was constructed stereoselectively by orthoester Claisen rearrangement of 8 followed by introduction of an isobutyl group. Basic treatment of the 15,23-diketone 12 followed by deprotection gave the title compound 2. 相似文献
119.
Y Nishikawa T Shindo K Ishii H Nakamura T Kon H Uno J Matsumoto 《Chemical & pharmaceutical bulletin》1989,37(5):1256-1259
A new series of oxopyridinecarboxamide derivatives 3a--g and 5a were synthesized and evaluated for their antiallergic activity. 1,4-Dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxamides 3a and 5a exhibited potent antiallergic activity (inhibitory rates of 80.7 and 88.3%, respectively, at 20 mg/kg, p.o.) in the rat passive cutaneous anaphylaxis (PCA) test and also exhibited much more potent in vitro inhibitory activity than caffeic acid against the enzyme 5-lipoxygenase (5-LO). Their in vitro antihistamine activity, however, was weaker than that of ketotifen. Compounds 3a and 5a are viewed as promising candidates for antiallergic agents. 相似文献
120.