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111.
Real spherical designs and real and complex projective designs have been shown by Delsarte, Goethals, and Seidel to give rise to association schemes when the strength of the design is high compared to its degree as a code. In contrast, designs on the complex unit sphere remain relatively uninvestigated, despite their importance in numerous applications. In this paper, we develop the notion of a complex spherical design and show how many such designs carry the structure of an association scheme. In contrast with the real spherical designs and the real and complex projective designs, these association schemes are nonsymmetric. 相似文献
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Hiroshi Tanaka Prof. Dr. Sho Yamaguchi Atsushi Yoshizawa Dr. Motoki Takagi Dr. Kazuo Shin‐ya Dr. Takashi Takahashi Prof. Dr. 《化学:亚洲杂志》2010,5(6):1407-1424
In this report, we describe the stereoselective synthesis of a combinatorial library comprised of 16 deoxyhexasaccharides that are related to a landomycin A sugar moiety, based on an orthogonal deprotection strategy. The use of an olivosyl donor containing a benzyl ether at the C3 position and benzoyl ester at the C4 position, and the olivosyl donor, a naphthylmethyl ether, and a p‐nitrobenzylethyl or benzyl sulfonyl ester enabled the synthesis of a set of four diolivosyl units containing a hydroxyl group at the C3 or C4 position by a simple glycosylation and deprotection procedure. Using a phenylthio 2,3,6‐trideoxyglycoside, α‐selective glycosidation proceeded without anomerization of the 2,6‐dideoxy‐β‐glycosides. In addition, alkylhydroquinone and levulinoyl groups were found to be an effective set of orthogonal protecting groups for the anomeric position and a hydroxyl group. The coupling of all combinations of trisaccharide units in a β‐selective manner was accomplished by activation of the glycosyl imidate with I2 and Et3SiH. No cleavage of the acid‐labile 2,3,6‐trideoxyglycoside was observed under the conditions used for the reactions. Finally, all of the protected hexasaccharides were deprotected by hydrolysis of the esters, microwave (MW) assisted cleavage of the 2‐trimethylsilylethoxymethoxy (SEM) ether, and a Birch reduction. 相似文献
115.
Sho Hirai 《Tetrahedron letters》2010,51(38):5076-5079
This Letter describes an enantioselective approach to (−)-platencin. A uniquely functionalized chiral intermediate, which was prepared via the highly enantioselective catalytic asymmetric intramolecular cyclopropanation (CAIMCP) that we have developed, was successfully transformed to Nicolaou’s intermediate in his total synthesis of (−)-platencin. 相似文献
116.
Kitade M Tanaka H Oe S Iwashima M Iguchi K Takahashi T 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(5):1368-1376
The solid-phase synthesis of a combinatorial cross-conjugated dienone library based on the structure of clavulones and their biological activity are reported. Clavulones are a family of marine prostanoids, and are composed of a cross-conjugated dienone system bearing two alkyl side-chains. The cross-conjugated dienone system irreversibly reacted with two nucleophiles. Our strategy for the solid-phase synthesis of the cross-conjugated dienones involves the Sonogashira-coupling reaction of a solid-supported cyclopentenone 10 bearing an acetylene group, followed by aldol condensation with aldehydes. The diphenyl derivative 7 aA was prepared from the solid-supported cyclopentenone 10 in 56% total yield. Combinatorial synthesis of a small library using twelve halides and eight aldehydes resulted in the production of 74 desired compounds from 98 candidates, and were detected by their mass spectra. Antiproliferative effects of the crude compounds against HeLaS3 cells showed that eleven samples showed strong antitumor activity (IC50<0.05 microM). Further biological examination of four purified compounds by using five tumor cell lines (A549, HeLaS3, MCF7, TMF1, and P388) revealed strong cytotoxicity comparable to that of adriamycin. 相似文献
117.
Ichihara Mai Inoue Kazumasa Fukushi Masahiro Shimizu Hideo Tsuruoka Hiroshi Veerasamy Nimelan Tsukada Mizuho Soyama Sho Hosokawa Shota Kato Tatsuki Sagara Hiroaki Taguchi Yoshiaki Natarajan Thennaarassan 《Journal of Radioanalytical and Nuclear Chemistry》2021,329(1):427-435
Journal of Radioanalytical and Nuclear Chemistry - Tokatsu area was on one pathway of the radioactive plumes released in the Fukushima Daiichi Nuclear Power Plant accident and absorbed dose rate in... 相似文献
118.
Kanna Adachi Sho Hasegawa Kazuaki Katakawa Takuya Kumamoto 《Tetrahedron letters》2017,58(47):4479-4482
We report the asymmetric total synthesis of (+)-blennolide C and (+)-gonytolide C isolated from endophytic fungi. The synthesis involved construction of a spirochromanone with a chiral quaternary carbon by the aldol reaction of o-hydroxyacetophenones and optically active α-oxygenated cyclohexenone, followed by cyclization under acidic conditions. Oxidative cleavage of the alkene moiety of the spirochromanone furnished the chromanone diester. Through treating the diester with a Lewis acid, the first total synthesis of (+)-blennolide C was achieved by deprotecting the oxygen functionality of the diester and simultaneous Dieckmann condensation. Total synthesis of (+)-gonytolide C was also achieved by lactone formation from the deprotected diester. 相似文献
119.
Dihydrosilanes undergo double trans-hydrosilylation with 1,4-diarylbuta-1,3-diynes in the presence of a cationic ruthenium catalyst to afford 2,5-diarylsiloles: in particular, 9-silafluorene is a good hydrosilylating agent to produce spiro-type siloles in good yield. 相似文献
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