全文获取类型
收费全文 | 2047篇 |
免费 | 52篇 |
国内免费 | 7篇 |
专业分类
化学 | 1705篇 |
晶体学 | 21篇 |
力学 | 23篇 |
数学 | 63篇 |
物理学 | 294篇 |
出版年
2021年 | 11篇 |
2020年 | 22篇 |
2019年 | 22篇 |
2018年 | 18篇 |
2017年 | 11篇 |
2016年 | 35篇 |
2015年 | 30篇 |
2014年 | 57篇 |
2013年 | 70篇 |
2012年 | 96篇 |
2011年 | 120篇 |
2010年 | 66篇 |
2009年 | 63篇 |
2008年 | 115篇 |
2007年 | 127篇 |
2006年 | 112篇 |
2005年 | 112篇 |
2004年 | 118篇 |
2003年 | 87篇 |
2002年 | 101篇 |
2001年 | 45篇 |
2000年 | 39篇 |
1999年 | 23篇 |
1998年 | 18篇 |
1997年 | 24篇 |
1996年 | 22篇 |
1995年 | 15篇 |
1994年 | 20篇 |
1993年 | 13篇 |
1992年 | 26篇 |
1991年 | 24篇 |
1990年 | 24篇 |
1989年 | 16篇 |
1988年 | 19篇 |
1987年 | 21篇 |
1986年 | 15篇 |
1985年 | 35篇 |
1984年 | 36篇 |
1983年 | 21篇 |
1982年 | 34篇 |
1981年 | 35篇 |
1980年 | 27篇 |
1979年 | 19篇 |
1978年 | 19篇 |
1977年 | 16篇 |
1976年 | 16篇 |
1975年 | 10篇 |
1974年 | 14篇 |
1973年 | 10篇 |
1968年 | 11篇 |
排序方式: 共有2106条查询结果,搜索用时 15 毫秒
91.
Yoshihiko Ito Yoshinori Inubushi Toru Sugaya Takeo Saegusa 《Journal of organometallic chemistry》1977,137(1):1-9
Reaction of carboxamides with Cu2O in the presence of t-butyl isocyanide gave new chelated copper(I) complexes, which probably are formed by the insertion of t-butyl isocyanide into the coppernitrogen bond of copper(I) amide isonitrile complexes, which were initially produced from the carboxamides and Cu2Ot-butyl isocyanide complex. The same chelated copper(I) complexes were prepared more readily by the reaction of the corresponding N-trimethylsilyl-carboxamides with Cu2Ot-butyl isocyanide complex. Reactions of the copper(I) complexes thus obtained with alkylating agents, such as alkyl halides, alkyl tosylates and triethyloxonium tetrafluoroborate, also were described. 相似文献
92.
The reaction of ortho-alkynylated benzaldehydes 1 with allyltrimethylsilane under the Pd(OAc)2-CuCl2 catalyst system gave the isochromene derivatives 2 together with the chlorinated products 3. When the reaction was conducted in the presence of half equiv of H2O, the formation of 3 was suppressed and 2 was obtained in good to high yields. When the reaction of 1a was carried out with trimethylsilylcyanide instead of allylsilane, the cyano group-substituted isochromene 9 was obtained in 94% yield. 相似文献
93.
Ishizaka T Miyanaga Y Mukai J Asaka K Nakai Y Tsuji E Uchida T 《Chemical & pharmaceutical bulletin》2004,52(8):943-948
The purpose of this study was to evaluate the bitterness of 18 different antibiotic and antiviral drug formulations, widely used to treat infectious diseases in children and infants, in human gustatory sensation tests and using an artificial taste sensor. Seven of the formulations were found to have a bitterness intensity exceeding 1.0 in gustatory sensation tests (evaluated against quinine as a standard) and were therefore assumed to have an unpleasant taste to children. The bitterness intensity scores of the medicines were examined using suspensions in water or an acidic sports drink. In the case of three macrolide antibiotic formulations containing erythromycin (ERYTHROCIN dry syrup), clarithromycin (CLARITH dry syrup for pediatric), and azithromycin (ZITHROMAC fine granules for pediatric use), the bitterness intensities of suspensions in acidic sports drinks were dramatically enhanced compared with the corresponding scores of suspensions in water. This enhancement could be predicted using the taste sensor. On the other hand, a reduction of bitterness intensity was observed for an acidic sports drink suspension of an amantadine product (SYMMETREL fine granules) compared with an aqueous suspension. This reduction in bitterness could also be predicted using the taste sensor output value. Thus, the taste sensor could predict whether or not suspension in an acidic sports drink would enhance or reduce the bitterness intensity of pediatric drug formulations, compared with suspensions in water. 相似文献
94.
Jiro Tsuji Toshiro Yamada Mitsumasa Kaito Tdakatsu Mandai 《Tetrahedron letters》1979,20(24):2257-2260
Regioselective aldol condensation of 2-octanone and 2-butanone at the methyl side proceeded in high yields using a system of dialkylaluminum phenoxide/tertiary amine. The intramolecular aldol condensation of 2,15-hexadecanedione was carried out by the same system, especially di-i-butylaluminum phenoxide/pyridine, to give dehydromuscone in 65% yield. Its hydrogenation afforded muscone (3-methylcyclopentadecanone). 相似文献
95.
Asao N Takahashi K Lee S Kasahara T Yamamoto Y 《Journal of the American Chemical Society》2002,124(43):12650-12651
The reaction of o-alkynylbenzaldehydes 1 and alkynes 2 in the presence of a catalytic amount of AuCl3 in (CH2Cl)2 at 80 degrees C gave naphthyl ketone products in high yields. The AuCl3-catalyzed formal [4 + 2] benzannulation proceeds most probably through the coordination of the triple bond of 1 to AuCl3, the formation of benzo[c]pyrylium auric ate complex via the nucleophilic addition of the carbonyl oxygen atom, the Diels-Alder addition of alkynes 2 to the auric ate complex, and subsequent bond rearrangement. Similarly, the AuCl3-catalyzed reactions of o-alkynylacetophenone and o-alkynylbenzophenone with phenylacetylene afforded the corresponding naphthyl ketone products in good yields. 相似文献
96.
Ando K Tsuji E Ando Y Kunitomo J Kobayashi R Yokomizo T Shimizu T Yamashita M Ohta S Nabe T Kohno S Ohishi Y 《Organic & biomolecular chemistry》2005,3(11):2129-2139
Variable benzo[b]furan derivatives having (E)- and (Z)-2-alkylcarbamoyl-1-methylvinyl groups at the 2-, 4- and 5-positions and a carboxylpropoxy or (1-phenyl)ethoxy group at the 7-position were prepared to find novel and selective leukotriene B4(LTB4) receptor antagonists. (E)-2-(2-diethylcarbamoyl-1-methylvinyl)-7-(1-phenylethoxy)benzo[b]furan (4v) showed selective inhibition to the human BLT2 receptor (hBLT2). On the other hand, (E)-2-acetyl-4-(2-diethylcarbamoyl-1-methylvinyl)-7-(1-phenylethoxy)benzo[b]furan (7v) inhibited both human BLT(1) receptor (hBLT1) and hBLT2. The (E)-2-(2-diethylcarbamoyl-1-methylvinyl) group lay on approximately the same plane as the benzo[b]furan ring, whereas the (E)-4-(2-diethylcarbamoyl-1-methylvinyl) group had the torsion angle (45.7 degree) from the benzo[b]furan ring plane. However, the (Z)-(2-alkylcarbamoyl-1-methylvinyl)benzo[b]furans were inactive. The inhibitory activity depended on the conformation of the 2-diethylcarbamoyl-1-methylvinyl group. 相似文献
97.
Suzuki T Higuchi H Ohkita M Tsuji T 《Chemical communications (Cambridge, England)》2001,(17):1574-1575
Upon oxidative dimerization of pale yellow Ar2C=CHPh 1 (Ar = 4-Me2NC6H4), deep blue 1,4-dication 2(2+) was obtained as a stable salt, which was transformed into 1 by reductive C-C bond fission; deprotonation of 2(2+) gave intense yellow diene 3, which was interconvertible with violet dication 4(2+) by two-electron transfer, thus exhibiting two distinct modes of electrochromism before and after proton transfer. 相似文献
98.
Summary Selective and sensitive procedures are described for the direct differential pulse polarographic determination of antimony(III), indium(III) and cadmium(II) in propylene carbonate. This method was based on the salting-out extraction of their halide complexes into the solvent from acidic aqueous media. The extracted Sb(III), In(III) and Cd(II) complexes exhibit sharp differential pulse polarographic peaks at –0.21 V, –0.63 V and –0.72 V vs. SCE in salted-out propylene carbonate phases respectively. The lower limits of determination are 5.0g for Sb(III), 0.6g for In(III), and 0.2g for Cd(II) in 10 ml of the organic phase. A number of foreign ions are eliminated through both processes of solvent extraction and polarography using propylene carbonate.
Propylencarbonat als Lösungsmittel für die Fällungs-Extraktion und die nachfolgende Differential-Puls-Polarographie
Zusammenfassung Selektive und empfindliche Verfahren für die direkte Bestimmung von Sb(III), In(III) und Cd(II) in Propylencarbonat mit Hilfe der Differential-Puls-Polarographie wurden beschrieben. Die vorliegende Methode beruht auf der Fällungs-Extraktion der Halogenid-Komplexe aus wäßrig-saurem Medium in das Lösungsmittel. Die extrahierten Komplexe des Sb(III), In(III) und Cd(II) ergeben scharfe Peaks bei –0,21 V, –0,63 V und –0,72 V gegen die Kalomelelektrode in den betreffenden Propylencarbonat-Phasen. Die unteren Grenzen der Bestimmungen liegen bei 5,0g Sb, 0,6g In bzw. 0,2g Cd in 10 ml organischer Phase. Eine Anzahl Fremdionen wird durch die beiden Prozesse der Extraktion und der Polarographie in Propylencarbonat ausgeschaltet.相似文献
99.
100.
Masaharu Tsuji Chikashi Yamagiwa Minoru Endoh Yukio Nishimura 《Chemical physics letters》1980,73(3):407-412
The extensive bands observed from the helium afterglow reaction of SO2 in the 250–540 nm region are assigned to the new SO+(A2Π-X2Πr) system produced from the He+/SO2 dissociative charge-transfer reaction at thermal energy. They had been erroneously interpreted as the SO+2 (C?-X?) system produced from He(23S)/SO2 Penning ionization. The spectroscopic constants for the SO+A2Π) and SO+(X2Πr) states were determined. 相似文献