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排序方式: 共有232条查询结果,搜索用时 15 毫秒
61.
Colton D. Payne Bastian Franke Mark F. Fisher Fatemeh Hajiaghaalipour Courtney E. McAleese Angela Song Carl Eliasson Jingjing Zhang Achala S. Jayasena Grishma Vadlamani Richard J. Clark Rodney F. Minchin Joshua S. Mylne K. Johan Rosengren 《Chemical science》2021,12(19):6670
Head-to-tail cyclized peptides are intriguing natural products with unusual properties. The PawS-Derived Peptides (PDPs) are ribosomally synthesized as part of precursors for seed storage albumins in species of the daisy family, and are post-translationally excised and cyclized during proteolytic processing. Here we report a PDP twice the typical size and with two disulfide bonds, identified from seeds of Zinnia elegans. In water, synthetic PDP-23 forms a unique dimeric structure in which two monomers containing two β-hairpins cross-clasp and enclose a hydrophobic core, creating a square prism. This dimer can be split by addition of micelles or organic solvent and in monomeric form PDP-23 adopts open or closed V-shapes, exposing different levels of hydrophobicity dependent on conditions. This chameleonic character is unusual for disulfide-rich peptides and engenders PDP-23 with potential for cell delivery and accessing novel targets. We demonstrate this by conjugating a rhodamine dye to PDP-23, creating a stable, cell-penetrating inhibitor of the P-glycoprotein drug efflux pump.The cyclic peptide PDP-23 adopts a different structure depending on conditions. In water it forms a dimer, but can unfold allowing its hydrophobic core to interact with membranes. PDP-23 shows promise as a cell penetrating scaffold for drug delivery. 相似文献
62.
Beck BJ Aldrich CC Fecik RA Reynolds KA Sherman DH 《Journal of the American Chemical Society》2003,125(41):12551-12557
The unique ability of the pikromycin (Pik) polyketide synthase to generate 12- and 14-membered ring macrolactones presents an opportunity to explore the fundamental processes underlying polyketide synthesis, specifically the mechanistic details of the chain extension process. We have overexpressed and purified PikAIII (module 5) and PikAIV (module 6) and assessed the ability of these proteins to generate tri- and tetraketide lactone products using N-acetylcysteamine-activated diketides and (14)C-methylmalonyl-CoA as substrates. Comparison of the stereochemical specificities for PikAIII and PikAIV and the reported values for the DEBS modules reveals significant differences between these systems. 相似文献
63.
64.
Haiwen Zhang Jennifer E. Enman Maren L. Conrad Marcy J. Manning Courtney S. Turner Susan L. Wheaton Christopher M. Vogels Stephen A. Westcott Andreas Decken Felix J. Baerlocher 《Transition Metal Chemistry》2006,31(1):13-18
Pyridinecarboxaldimines (N–N′) derived from pyridin-2-ylcarboxaldehydes and unsaturated amines add to [PdCl2(coe)]2 (coe = cis-cyclooctene) to give complexes of the type PdCl2(N–N′) in moderate yields. The palladium complexes have been investigated as substrates for hydroboration reactions and as
antifungal agents against Aspergillus niger, A. flavus, Candida albicans, and Saccharomyces cerevisiae. 相似文献
65.
Amanda C. Evans Jared Skey Megan Wright Wenjun Qu Courtney Ondeck Deborah A. Longbottom Rachel K. O'Reilly 《Journal of polymer science. Part A, Polymer chemistry》2009,47(24):6814-6826
We report the application of reversible addition‐fragmentation chain transfer polymerization using a novel chain transfer agent toward the synthesis of a variety of copolymers containing proline‐derived monomeric units. This methodology enables ready access to a number of polymeric species with narrow molecular weight distributions, reliable functional unit incorporations, and high conversions. The methodology is also a facile approach to novel copolymeric species incorporating amino acids, which possess unique material properties and the potential for further organocatalytic application. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009 相似文献
66.
The behaviour ofS-matrix for potentials generating bound states in continuum in the neighbourhood of the positive bound state energies is studied.
It is shown that unlike the case of usual negative energy bound states, theS-matrix does not have a pole at the positive bound state energy but becomes unity at the energy corresponding to bound states
in continuum. Calculations ofS-waveS-matrix for a local potential constructed by Stillinger and Herrick and a separable nonlocal potential constructed by the
present authors verify these results. Our results indicate that the bound states embedded in continuum constructedvia the von Neumann and Wigner procedure cannot be interpreted as resonances with zero width. 相似文献
67.
Sessler JL Jayawickramarajah J Sherman CL Brodbelt JS 《Journal of the American Chemical Society》2004,126(37):11460-11461
A pyrrole-appended purine nucleoside 1 is described that can form an "extended" three-point Hoogsteen-type interaction due to the stabilization of the donor-acceptor-acceptor (DAA) motif. Nucleoside 1 is shown to bind guanosine 10 (a classic ADD motif) to form ensemble I. This interaction competes effectively with guanosine self-assembly and, as such, is capable of disrupting guanosine quadruplex formation. 相似文献
68.
Luchaco-Cullis CA Mizutani H Murphy KE Hoveyda AH 《Angewandte Chemie (International ed. in English)》2001,40(8):1456-1460
69.
70.
Copper iodide was utilized as a relatively inexpensive catalyst for the synthesis of podocarpic acid ether derivatives in excellent yields through the one-step cross-coupling reaction of methyl 13-iodo-O-methylpodocarpate with alcohols. 相似文献