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131.
132.
Ohashi M Takeda I Ikawa M Ogoshi S 《Journal of the American Chemical Society》2011,133(45):18018-18021
Pyridines, which comprise one of the most important classes of the six-membered heterocyclic compounds, are widely distributed in nature, and the transition-metal-catalyzed [2 + 2 + 2] cycloaddition reaction of two alkynes and a nitrile is one of the most powerful methods for preparing versatile, highly substituted pyridine derivatives. However, the lack of chemo- and regioselectivity is still a crucial issue associated with fully intermolecular [2 + 2 + 2] cycloaddition. The present study developed the Ni(0)-catalyzed intermolecular dehydrogenative [4 + 2] cycloaddition reaction of 1,3-butadienes with nitriles to give a variety of pyridines regioselectively. 相似文献
133.
Dr. Tomoki Ogoshi Daiki Yamafuji Takamichi Aoki Keisuke Kitajima Prof. Tada‐aki Yamagishi Yoshihiro Hayashi Dr. Susumu Kawauchi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(24):7493-7500
Planar chiral [2]‐ and [3]rotaxanes constructed from pillar[5]arenes as wheels and pyridinium derivatives as axles were obtained in high yield using click reactions. The process of rotaxane formation was diastereoselective; the obtained [2]rotaxane was a racemic mixture consisting of (pS, pS, pS, pS, pS) and (pR, pR, pR, pR, pR) forms of the per‐ethylated pillar[5]arene ( C2 ) wheel, and other possible types of the [2]rotaxane did not form. Isolation of the enantiopure [2]rotaxanes with one axle through (pS, pS, pS, pS, pS)‐ C2 or (pR, pR, pR, pR, pR)‐ C2 wheels was accomplished. Furthermore, pillar[5]arene‐based [3]rotaxane was successfully synthesized by attachment of two pseudo [2]rotaxanes onto a bifunctional linker. [3]Rotaxane formed in a 1:2:1 mixture with one axle threaded through two (pS, pS, pS, pS, pS)‐ C2 , one (pS, pS, pS, pS, pS)‐ C2 and one (pR, pR, pR, pR, pR)‐ C2 (meso form), or two (pR, pR, pR, pR, pR)‐ C2 wheels. The [3]rotaxane enantiomers and the meso form were successfully isolated using appropriate chiral HPLC column chromatography. The procedure developed in this study is the starting point for the creation of pillar[5]arene‐based interlocked molecules. 相似文献
134.
Kobayashi N Furuya F Yug GC Wakita H Yokomizo M Ishikawa N 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(6):1474-1484
Several cofacial phthalocyanines (Pcs) with an Si-Si linkage were obtained by one-step condensation of 1H-isoindole-1,3(2H)-diimine with hexachlorodisilane as template in quinoline. They were characterized by gel-permeation chromatography, IR, NMR spectroscopy, and mass spectrometry, and cyclic voltammetry. The results strongly suggest that we indeed obtained Pc dimers directly linked by an Si-Si bond using this novel concept of utilizing a compound/salt with an element-element bond as a template. The cofacial dimer structures are reasonably supported by X-ray absorption near-edge structure (XANES), electronic absorption and magnetic circular dichroism (MCD) spectra, and molecular orbital (MO) calculations. Interestingly, they show an electronic absorption spectrum very similar to that of silicon tetrabenztriazacorrole (SiTBC). 相似文献
135.
136.
Acetone, acetylacetone, and ethyl acetoacetate undergo facile and direct metallation at the α-positions of carbonyl groups with a cationic rhodium(III) porphyrin complex under mild conditions. 相似文献
137.
Ni(cod)(2)/P(t)Bu(3) system catalyzed the dimerization of terminal alkynes to give (E)-head-to-head dimerization products, in which the stannylacetylene dimer could be applied to a one-pot synthesis of a conjugated enyne, when combined with Migita-Stille coupling. 相似文献
138.
Separation of Linear and Branched Alkanes Using Host–Guest Complexation of Cyclic and Branched Alkane Vapors by Crystal State Pillar[6]arene 下载免费PDF全文
Prof. Tomoki Ogoshi Kazuki Saito Ryuta Sueto Ryosuke Kojima Yukie Hamada Prof. Shigehisa Akine Dr. Adhitya Mangala Putra Moeljadi Dr. Hajime Hirao Dr. Takahiro Kakuta Prof. Tada‐aki Yamagishi 《Angewandte Chemie (International ed. in English)》2018,57(6):1592-1595
Activated crystals of pillar[6]arene produced by removing the solvent upon heating were able to take up branched and cyclic alkane vapors as a consequence of their gate‐opening behavior. The uptake of branched and cyclic alkane vapors by the activated crystals of pillar[6]arene induced a crystal transformation to form one‐dimensional channel structures. However, the activated crystals of pillar[6]arene hardly took up linear alkane vapors because the cavity size of pillar[6]arene is too large to form stable complexes with linear alkanes. This shape‐selective uptake behavior of pillar[6]arene was further utilized for improving the research octane number of an alkane mixture of isooctane and n‐heptane: interestingly, the research octane number was dramatically improved from a low research octane number (17 %) to a high research octane number (>99 %) using the activated crystals of pillar[6]arene. 相似文献
139.
Sensuke Ogoshi 《Journal of organometallic chemistry》2004,689(3):662-665
Homoleptic olefin platinum(0) complexes, Pt(C7H10)3 and Pt(cod)2, were synthesized by the colorimetric reduction of platinum(II) complexes with SmI2 in the presence of 2-norbornene or COD. This is a practically more convenient method for the synthesis of the Pt(0) complexes than the literature method employing Li2(cot). 相似文献
140.
Shixin Fa Keisuke Adachi Yuuya Nagata Kouichi Egami Kenichi Kato Tomoki Ogoshi 《Chemical science》2021,12(10):3483
Regulating the chirality of macrocyclic host molecules and supramolecular assemblies is crucial because chirality often plays a role in governing the properties of these systems. Herein, we describe pillar[5]arene-based chiral nanotube formation via pre-regulation of the building blocks'' chirality, which is different from frequently used post-regulation strategies. The planar chirality of rim-differentiated pillar[5]arenes is initially regulated by chiral awakening and further induction/inversion through stepwise achiral external stimuli. The pre-regulated chiral information is well stored in discrete nanotubes by interacting with a per-alkylamino-substituted pillar[5]arene. Such pre-regulation is more efficient than post-regulating the chirality of nanotubes.Pillar[5]arene-based chiral nanotube formation via pre-regulation of the building blocks'' chirality is more efficient than post-regulating the chirality of nanotubes. 相似文献