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1.
《Mendeleev Communications》2022,32(3):395-396
A new method for assembling 1,3-selenazolines by the iodine- mediated reaction of the simplest building blocks such as elemental selenium, alkenes and acetonitrile has been discovered. A proposed mechanism includes the addition of the intermediate selenium iodides to alkene with subsequent solvent interception by the formed seleniranium ion. 相似文献
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A novel methodology for the regio- and stereoselective synthesis of amino alcohol derivatives from allylalcohols/ethers via intramolecular nucleophilic participation by the sulfilimine moiety is disclosed. The sulfilimine moiety is stereospecifically transformed to a sulfinyl moiety with an inverted configuration. The reaction is general and affords highly functionalised products. 相似文献
4.
Colin Eaborn Anna Kowalewska Wlodzimierz Stanczyk 《Journal of organometallic chemistry》1998,560(1-2)
The finding that compounds of the type (Me3Si)2(PhMe2Si)CSiMePhX react with electrophiles to give very predominantly rearranged products (Me3Si)2(Ph2MeSi)CSiMe2Y, which would be expected to be thermodynamically disfavoured, can be rationalized in terms of a mechanism in which the anchimerically-assisted departure of X− gives the Ph-bridged cation [(Me3Si)2
MePh]+ which is attacked by the nucleophile at the less hindered centre bearing two Me groups rather than that bearing one Me and one Ph group, with the outcome determined by kinetic rather than thermodynamic factors. Both (Me3Si)2(Ph2MeSi)CSiMe2Br and its isomer (Me3Si)2(PhMe2Si)CSiMePhBr react with AgBF4 in CH2Cl2 or Et2O to give >95% of the fluoride (Me3Si)2(Ph2MeSi)CSiMe2F. Reaction of the bromide (Me3Si)2(PhMe2Si)CSiMePhBr with AgO2CCF3 in Et2O, and that of the hydride (Me3Si)2(PhMe2Si)CSiMePhH with ICl in CCl4, likewise give >95% of the rearranged (Me3Si)2(Ph2MeSi)CSiMe2O2CCF3 and (Me3Si)2(Ph2MeSi)CSiMe2Cl, respectively. 相似文献
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Copper(I) catalysts are usually ineffective on the other hand Pd(II) catalysts are quite effective in promoting intramolecular sp2 C–H functionalization (C–S bond formation). Herein, we have developed a ligand assisted Pd(II) catalyzed C–S bond formation via C–H activation from arylthioureas leading to the formation of 2-aminobenzothiazoles for substrates bearing electron donating (EDG) groups in the aryl ring. However without the assistance of ligand this Pd(II) catalyzed reaction is quite unproductive particularly for thioureas possessing strongly electron donating groups in the aryl rings. Interestingly, the ligand free Cu(II) catalyzed oxidative cyclization of arylthioureas are equally effective both for arylthioureas possessing electron donating as well as electron withdrawing groups in the aryl rings. 相似文献
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Nickel‐Catalyzed C?H Alkylations: Direct Secondary Alkylations and Trifluoroethylations of Arenes 下载免费PDF全文
Weifeng Song Sebastian Lackner Lutz Ackermann 《Angewandte Chemie (International ed. in English)》2014,53(9):2477-2480
A versatile nickel catalyst allowed for C H alkylations of unactivated arenes with challenging secondary alkyl bromides and chlorides. The high catalytic efficacy also set the stage for direct secondary alkylations of indoles as well as C H trifluoroethylations with ample substrate scope. 相似文献
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Convenient conditions for the Stille coupling of halide‐bearing triorganotin compounds, which do not normally react under typical Stille reaction conditions, are presented. The coupling of vinylstannanes with allyl bromide using palladium(II) catalysis is accomplished under fluoride assistance to give the substituted 2,5‐hexadien‐1‐ols in Z‐configuration. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
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Iododesilylation of trisubstituted (Z)-silyl olefins proceeds with retention of geometry in hexafluoroisopropanol (HFIP) but, for unhindered cases, with inversion of geometry in DMSO. When an acyloxy substituent is positioned to participate in the reaction, the protocol consistently leads to inversion of geometry. 相似文献
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Based on a calculation model,we study the interference phenomena of serially coupled V-type and Λ-type triple quantum dots (CTQDs) driven simultaneously by a strong driving field and a weak probe field.Strongly depending on the configuration of the three-level CTQD,the probe absorption spectra,which are shown in the tunneling current,exhibit various quantum coherence properties.In the case where the two pairs of transitions of the CTQD have a small eigenfrequency difference △ω,the double-coupling effect of the driving field results in two Autler-Townes doublets and one weak Mollow triplet in one spectrum.With the value of △ω increasing,only one Autler-Townes splitting remains due to the single-coupling of the field.We also find that the effect of spontaneous emission of phonons may lead to an obvious background current,which can be used to distinguish which transition is driven by the driving field in experiment.The interesting quantum property of a CTQD revealed in our results suggests its potential applications in quantum modulators and quantum logic devices. 相似文献
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以实验技术人员的视角,从不同实验环节出发,全面总结实验辅助工作,并提炼为实验辅助大三部曲和小三部曲。该方面的工作体系源于实验室开设的"化学生物学综合实验",反哺了实验室多门实验课程,取得了良好的效果,促进了实验教学质量的提升,同时也为环境育人创造了有利的条件。 相似文献