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排序方式: 共有49条查询结果,搜索用时 15 毫秒
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Roe C Moragas Solá T Sasraku-Neequaye L Hobbs H Churcher I MacPherson D Stockman RA 《Chemical communications (Cambridge, England)》2011,47(26):7491-7493
The synthetic utility of S-mesitylsulfinimines for the synthesis of chiral amines and aziridines was examined through their reactions with Grignard reagents, with the ylides derived from trimethylsulfonium iodide and S-allyl-tetrahydrothiophenium bromide and through an aza-Darzens manifold, affording convenient access to a diverse range of highly substituted chiral amines and aziridines in high yields and excellent stereoselectivities. 相似文献
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Ronald Grigg William S. MacLachlan David T. MacPherson Visuvanathar Sridharan Selvaratnam Suganthan 《Tetrahedron》2001,57(52):10335-10345
Up to four bonds and five stereocentres are created, in five component processes (five point diversity), utilising resin bound aryl iodides by hydroboration or hydrostannylation of alkynes, followed by cyclisation–anion capture involving Suzuki or Stille reactions. Three small libraries were prepared to validate the chemistry. 相似文献
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S. S. Selliah S. Cussion K. A. MacPherson E. J. Reiner D. Toner 《Analytical and bioanalytical chemistry》2001,370(2-3):208-212
Matrix–matched environmental certified reference materials (CRMs) are one of the most useful tools to validate analytical methods, assess analytical laboratory performance and to assist in the resolution of data conflicts between laboratories. This paper describes the development of a lake sediment as a CRM for polychorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) and dioxin-like polychlorinated biphenyls (DLPCBs). The presence of DLPCBs in the environment is of increased concern and analytical methods are being developed internationally for monitoring DLPCBs in the environment. This paper also reports the results of an international interlaboratory study involving thirty-five laboratories from seventeen countries, conducted to characterize and validate levels of a sediment reference material for PCDDs, PCDFs and DLPCBs. 相似文献
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Silva-López M Fender A MacPherson WN Barton JS Jones JD Zhao D Dobb H Webb DJ Zhang L Bennion I 《Optics letters》2005,30(23):3129-3131
We have measured the optical phase sensitivity of fiber based on poly(methyl methacrylate) under near-single-mode conditions at 632.8 nm wavelength. The elongation sensitivity is 131 +/- 3 x 10(5) rad m(-1) and the temperature sensitivity is -212 +/- 26 rad m(-1) K(-1). These values are somewhat larger than those for silica fiber and are consistent with the values expected on the basis of the bulk polymer properties. 相似文献
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Philip Wiredu Addo Sai Uday Kumar Reddy Sagili Samuel Eichhorn Bilodeau Frederick-Alexandre Gladu-Gallant Douglas A. MacKenzie Jennifer Bates Garnet McRae Sarah MacPherson Maxime Paris Vijaya Raghavan Valrie Orsat Mark Lefsrud 《Molecules (Basel, Switzerland)》2022,27(24)
Limited studies have explored different extraction techniques that improve cannabis extraction with scale-up potential. Ultrasound-assisted and microwave-assisted extraction were evaluated to maximize the yield and concentration of cannabinoids and terpenes. A central composite rotatable design was used to optimize independent factors (sample-to-solvent ratio, extraction time, extraction temperature, and duty cycle). The optimal conditions for ultrasound- and microwave-assisted extraction were the sample-to-solvent ratios of 1:15 and 1:14.4, respectively, for 30 min at 60 °C. Ultrasound-assisted extraction yielded 14.4% and 14.2% more oil and terpenes, respectively, compared with microwave-assisted extracts. Ultrasound-assisted extraction increased cannabinoid concentration from 13.2–39.2%. Considering reference ground samples, tetrahydrocannabinolic acid increased from 17.9 (g 100 g dry matter−1) to 28.5 and 20 with extraction efficiencies of 159.2% and 111.4% for ultrasound-assisted and microwave-assisted extraction, respectively. Principal component analyses indicate that the first two principal components accounted for 96.6% of the total variance (PC1 = 93.2% and PC2 = 3.4%) for ultrasound-assisted extraction and 92.4% of the total variance (PC1 = 85.4% and PC2 = 7%) for microwave-assisted extraction. Sample-to-solvent ratios significantly (p < 0.05) influenced the secondary metabolite profiles and yields for ultrasound-assisted extracts, but not microwave-assisted extracts. 相似文献