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2017, Third edition., ISBN 9781476667775, xv, 379 pages
"In its updated and expanded third edition, this reference work provides hundreds of fascinating facts about libraries, books, periodicals, reference... 
Information resources | Libraries | Books | Information services
Book
Inorganic Chemistry, ISSN 0020-1669, 10/2015, Volume 54, Issue 20, pp. 9833 - 9844
When n-hexane solutions of an excess of sodium bis­(trimethylsilyl)­amide (NaHMDS) are combined with cesium halide (halide = Cl, Br, or I) in the presence of... 
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 08/2018, Volume 156, pp. 800 - 814
A number of 5-arylisatin derivatives were synthesized in 5–6 steps from readily available starting materials. Their structures were confirmed by 1H NMR and 13C... 
Angiogenesis | Synthesis | Proliferation | 5-phenylisatin | Migration | NQWUPWUECPPGIW-UHFFFAOYSA-N | ANLTXNNMSRCHCN-UHFFFAOYSA-N | PUNXJSZLFZQUAB-UHFFFAOYSA-N | VZNYACKYPSHSOU-UHFFFAOYSA-N | BHXSWBKMTUVULL-UHFFFAOYSA-N | DVVYNKPDVYRUCX-UHFFFAOYSA-N | HNLCFABWVBXZCD-UHFFFAOYSA-N | NLVWVQNXXBRNSF-UHFFFAOYSA-N | KFRCELJAQDCUFU-UHFFFAOYSA-N | LJIWGGIBHLOGIV-UHFFFAOYSA-N | KLRYXALRASRZSZ-UHFFFAOYSA-N | UZZKXZMLRJPWHY-UHFFFAOYSA-N | WJBPAFLRNLASSA-QRQIAZFYSA-N | WMKGTZOSXSVDFZ-UHFFFAOYSA-N | SRKOXUDYFFCIAD-UHFFFAOYSA-N | QRKGJDJKKVZLJZ-UHFFFAOYSA-N | ZDGMYXUBGVOAKW-UHFFFAOYSA-N | JNYHNYANZWQCGQ-UHFFFAOYSA-N | BMANTURQBSXOFX-UHFFFAOYSA-N | DRYRGMFBQMGXPB-UHFFFAOYSA-N | NUAMVJIXZFIQKX-UHFFFAOYSA-N | CALZDBFRPMTDQT-GYHWCHFESA-N | NDFUGRNSKABAHC-UHFFFAOYSA-N | DGSRGVDBCLLEQZ-JLPGSUDCSA-N | SCYQIRIBDBKXGG-UHFFFAOYSA-N | GLXDXOJIIXNBFX-UHFFFAOYSA-N | ORJDUBSLXFDEKU-UHFFFAOYSA-N | HMTMIKQLZXMAMT-UHFFFAOYSA-N | WOZYGCUDNFSAMU-UHFFFAOYSA-N | CGVRMPCDBYRPGV-UHFFFAOYSA-N | SZCKMTCYVDYGEB-UHFFFAOYSA-N | RKRAVBKCNMIBIK-UHFFFAOYSA-N | NFEWGBYJTMAOAE-UHFFFAOYSA-N | YIEYFAOUUYBIEG-UHFFFAOYSA-N | XQIGYJUCWBVHDV-UHFFFAOYSA-N | BOWDQFHYUWMVSK-UHFFFAOYSA-N | QJYUXPHANUMTLA-UHFFFAOYSA-N | JNWCIWDOWAVNEX-UHFFFAOYSA-N | MURNNTGIMOTEEI-UHFFFAOYSA-N | PQDURQOFPGFUFH-UHFFFAOYSA-N | LLGKXCGBYQERAR-UHFFFAOYSA-N | OEQVJYYMYNMBQR-UHFFFAOYSA-N | ZIFMYEUABOAUPY-UHFFFAOYSA-N | KKNIRCSVMWWEOY-UHFFFAOYSA-N | WPZWOMJBXSCVQY-UHFFFAOYSA-N | SZSAXLRFQKXWLL-UHFFFAOYSA-N | CGOUNXKCEGEARF-HAHDFKILSA-N | ZHYYSTBSIDKXEP-UHFFFAOYSA-N | JEAPPFRTYMXSOT-UHFFFAOYSA-N | RKCYEFAWSDGUSD-UHFFFAOYSA-N | VDJZRQWVBSDWGQ-UHFFFAOYSA-N | DPJQRIMBZXQXMJ-DXJNIWACSA-N | JGIUEALCJPSECX-UHFFFAOYSA-N | WXCWDAWGTWQPIB-VEILYXNESA-N | YNUKUKBQZLCNHO-UHFFFAOYSA-N | YRBIKCXVGGTAKX-UHFFFAOYSA-N | JPCMFBGBNFEZBC-UHFFFAOYSA-N | HDMORQPPXMLTHL-UHFFFAOYSA-N | APOPTOSIS | DESIGN | CHEMISTRY, MEDICINAL | DOCKING | ISATIN DERIVATIVES | INHIBITORS | Human Umbilical Vein Endothelial Cells | Leukemia - pathology | Apoptosis - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Isatin - pharmacology | Leukemia - metabolism | Isatin - chemistry | Neovascularization, Pathologic - pathology | Liver Neoplasms - pathology | Antineoplastic Agents - pharmacology | Angiogenesis Inhibitors - chemical synthesis | Liver Neoplasms - drug therapy | Angiogenesis Inhibitors - pharmacology | Leukemia - drug therapy | Antineoplastic Agents - chemistry | Hep G2 Cells | Cell Movement - drug effects | Isatin - chemical synthesis | Neovascularization, Pathologic - drug therapy | K562 Cells | Liver Neoplasms - metabolism | Cell Proliferation - drug effects | Angiogenesis Inhibitors - chemistry | Drug Screening Assays, Antitumor | Prevention | Antimitotic agents | Liver cancer | Liver | Leukemia | Antineoplastic agents | Cancer
Journal Article
Hydrometallurgy, ISSN 0304-386X, 05/2017, Volume 169, pp. 576 - 584
A novel tridentate extractant including a soft donor has been developed and examined. The extractant, N,N,N′,N′-tetraoctyl-thiodiglycolamide (TDGA), is... 
Solvent extraction | MIDOA | TDGA | Soft donor | TODGA | METALLURGY & METALLURGICAL ENGINEERING | SILVER | LIQUID-LIQUID-EXTRACTION | SOLVENT-EXTRACTION | SELECTIVE EXTRACTANTS | COUNTER-CURRENT EXTRACTION | ACTINIDES | LIGAND | NITRIC-ACID | CALIXARENES | Silver | Cytokinins | Nitrogen | Analysis | Sulfur compounds | Nuclear energy
Journal Article
Tetrahedron, ISSN 0040-4020, 08/2018, Volume 74, Issue 32, pp. 4289 - 4294
The Diels-Alder reactivity of 1,2-heteroborines (H4C4B(H)X, X = NH, PH, AsH; O, S, Se) has been computationally explored by means of Density Functional Theory... 
1,2-Heteroborines | Diels-Alder | Reactivity | Aromaticity | Activation strain model | PONOWYVXWZVCCC-UHFFFAOYSA-N | SRHVNFUDFFIVRN-NUBCRITNSA-N | YCEGGNNGACCHFZ-UHFFFAOYSA-N | ZSTCCYWGIXBRPV-UHFFFAOYSA-N | NTNGMURAICZZPC-UHFFFAOYSA-N | QCUMWZDVNMRVET-DPYQTVNSSA-N | IOQJCJHBDWXZSD-LURJTMIESA-N | DTGYORVSPXZQBM-MOJAZDJTSA-N | VNAOUIBJUVIGLA-UHFFFAOYSA-N | CHKCLPJIWDOSQM-UHFFFAOYSA-N | UHOVQNZJYSORNB-UHFFFAOYSA-N | CLXFSILJZKQTSQ-DPYQTVNSSA-N | PGDUPBGRQSLJLK-UHFFFAOYSA-N | TVASWQMJDYUUIV-KVFPUHGPSA-N | PWZYIISNJZBZQV-UHFFFAOYSA-N | ZEXMUHQFTFFKEH-CJJZRWNGSA-N | CVNJOQLFFFUABC-UHFFFAOYSA-N | RQNTTXFSYWVJTC-UHFFFAOYSA-N | VCGYXDRALTWCFJ-FYZOBXCZSA-N | OGZZEGWWYQKMSO-UHFFFAOYSA-N | CLXFSILJZKQTSQ-MOJAZDJTSA-N | UMHSJEDRIIKSDA-ZETCQYMHSA-N | RWRJVRXWGGLQLS-UHFFFAOYSA-N | MEUCBUADBJJJIM-UHFFFAOYSA-N | VJFYALMMNXTWRN-UHFFFAOYSA-N | UJIZQFICYZHGNK-UHFFFAOYSA-N | RSGUYISAUVGSNH-UHFFFAOYSA-N | VXFHRPANTVCIPR-NRISCCJGSA-N | ZDPCTADKEKBXLZ-UHFFFAOYSA-N | WVGXAASCDWGORG-UHFFFAOYSA-N | DTGYORVSPXZQBM-DPYQTVNSSA-N | VCGYXDRALTWCFJ-UHFFFAOYSA-N | VMRUNHMEWAQXLH-RXMQYKEDSA-N | QCUMWZDVNMRVET-MOJAZDJTSA-N | BOVKNQHKMJRFDH-UHFFFAOYSA-N | ZEFWGXUSXKYOKS-ZETCQYMHSA-N | CDFJCQZIHBKYRZ-UHFFFAOYSA-N | VHAIUPZTODXARC-UHFFFAOYSA-N | AVJVLDDGYUJTPU-UHFFFAOYSA-N | NIPJKMZODYZYJG-LURJTMIESA-N | PYYOTYPDWAFLMT-ZCFIWIBFSA-N | GUSVGQFIPAJYNZ-UHFFFAOYSA-N | FPYJFEHAWHCUMM-UHFFFAOYSA-N | PROAEQOBVSNCIT-UHFFFAOYSA-N | JURIEQICPHEWPD-MOJAZDJTSA-N | VXFHRPANTVCIPR-CDRLLEPJSA-N | JURIEQICPHEWPD-DPYQTVNSSA-N | BUDIPYFWNYIQGI-UHFFFAOYSA-N | KMMASONFEWIHBO-UHFFFAOYSA-N | NOODIUXEUXWPLQ-LURJTMIESA-N | ISUNFWIKLIQVHH-UHFFFAOYSA-N | VBUPWSLICFIRTD-UHFFFAOYSA-N | ZEXMUHQFTFFKEH-WWGBPYKYSA-N | BORON | HYDROGENATION | S(N)2 REACTIONS | CHEMISTRY, ORGANIC | ENERGY DECOMPOSITION ANALYSIS | MULTIBOND REACTIONS | MOLECULAR-ORBITAL THEORY | CYCLOADDITION REACTION | SYNCHRONICITY | Density functionals | Specific gravity
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 12/2018, Volume 876, pp. 66 - 77
Bifunctional silanes ClCH2SiF3 and ClCH2SiF2Me react with N-trimethylsilyl-N-methylacetamide and its tautomer О-trimethylsilyl-N-methylacetimidate as ambident... 
Trans-silylation | Bifunctional (chloromethyl)fluorosilanes | N-trimethylsilyl-N-methylacetamide | O-trimethylsilyl-N-methylacetimidate | Alkylation | LZBXJLBYHFVKID-UHFFFAOYSA-N | GHULCXGKGMKDRP-YVFTVSHDSA-N | VNCINCFHIHBABX-UHFFFAOYSA-N | ZHMMUJBOBFHFGQ-FJXQXJEOSA-N | LEQPQYLSKOOZBC-OGFXRTJISA-N | NHVCXSOQGUQWPJ-UHDJGPCESA-N | DNZMWSMASHVUSH-UHFFFAOYSA-N | QZXIUIVNLBSEAV-SNVBAGLBSA-N | PXBXSQIAOCLLJL-XBXARRHUSA-N | IRKIANSIKSKTKR-VOTSOKGWSA-N | QHUOBLDKFGCVCG-UHFFFAOYSA-N | KJPHRQFOVIMVRY-SOFGYWHQSA-N | QHTVELKRMQXYEL-RMZRELHQSA-N | ZMQMFPJITFFNNN-UHFFFAOYSA-N | LYZQNNUMEMOAMJ-UHDJGPCESA-N | XVDDRRAIRVXXKL-UHFFFAOYSA-N | IJOOHPMOJXWVHK-UHFFFAOYSA-N | KMDJTGORMWBENH-XBXARRHUSA-N | LHMKUTKRLVWHGR-VMPITWQZSA-N | BUWVFXQXJZZXMB-JTQLQIEISA-N | CTIKAHQFRQTTAY-UHFFFAOYSA-N | GSSJYDPDBXWCQB-UHFFFAOYSA-N | KNBHNRSDNNQEDD-SOFGYWHQSA-N | HFYKLNXKBNFHFQ-UHFFFAOYSA-N | LBDKEDMWUNEPJA-KPKJPENVSA-N | YVAKMDBUZRKCCY-UHFFFAOYSA-N | JCCVPMDZJPSMKQ-QRPNPIFTSA-N | XZOLBVIGBYYFGV-UHFFFAOYSA-N | DQCRGAGEZPEQKW-VHODGJRUSA-N | OAAYVUOGEYBJKX-ZDTICIBISA-N | CWLUGSDHELAQNH-UHFFFAOYSA-N | GMVMMSWZWUKXFF-KMXZHCNGSA-N | QTEOOICTJFZYHL-XBXARRHUSA-N | PEELWXHICOPINM-UHFFFAOYSA-N | PPQLDFJGDNYQAV-SOFGYWHQSA-N | OVVYHHUTRRZFBO-UHFFFAOYSA-N | CHAMWPSLFQXIPT-UHFFFAOYSA-N | KATVUIAWELMJKD-UHFFFAOYSA-N | MZNJKFZRKLEMSZ-UHFFFAOYSA-N | PSYFYONVUBTXLR-UHDJGPCESA-N | YORSPWXYCHFRGC-UHFFFAOYSA-N | ICBLAYYRCPHQLM-UHFFFAOYSA-N | OIXFBORHATWXCM-UHFFFAOYSA-N | FPGLPOIMBLXJEY-UHFFFAOYSA-N | FESSCXXKADLNIV-YHNNWUSJSA-N | IGWTVVLXPBAHMC-UHFFFAOYSA-N | CRYSTAL-STRUCTURE | S(N)2 REACTIONS | REACTIVITY | CHEMISTRY, ORGANIC | INTRAMOLECULAR COORDINATION | CHEMISTRY, INORGANIC & NUCLEAR | REARRANGEMENT | SUBSTITUTED 2-PHENYLACETAMIDES | SILICON COMPLEXES | PENTACOORDINATE | DERIVATIVES | AMIDES | Amides | Nuclear magnetic resonance spectroscopy | Analysis | Silane
Journal Article
Inorganic Chemistry, ISSN 0020-1669, 11/2017, Volume 56, Issue 21, pp. 13140 - 13151
Journal Article
Journal of Catalysis, ISSN 0021-9517, 11/2016, Volume 343, pp. 240 - 247
[Display omitted] •Electrocarboxylation of 2,3-dimethyl-butadiene at an onset potential of −1.3V.•Elucidation of electrocarboxylation mechanism by first... 
Electrochemistry | Density functional theory | Nickel | Mechanism | Carbon dioxide | JCOADMTVEFEMRB-UHFFFAOYSA-N | DCWNMBVZNOMUIO-UHFFFAOYSA-L | KAXRPGOVDVRQRV-UHFFFAOYSA-N | RLERLEQTWMVLOE-UHFFFAOYSA-N | YCYXAVOSNLLCKA-UHFFFAOYSA-N | SUQIPZMRMITSOM-UHFFFAOYSA-N | VOHHNFLDCHAUIY-UHFFFAOYSA-N | Mmc1.pdf | LYNHTPHTJWVPKK-UHFFFAOYSA-N | MYPVOBFYUVCLMO-UHFFFAOYSA-N | QPVGPARGNKXDJE-UHFFFAOYSA-N | JFHMZJRGAJXOEP-UHFFFAOYSA-N | LABRWMOJSAYDPL-UHFFFAOYSA-N | BXCJKFHLMPZGKJ-UHFFFAOYSA-N | WFTITXXWBRVCLK-UHFFFAOYSA-M | JBLZCMLQVGGGBV-QDXJQGPWSA-N | KAKZBPTYRLMSJV-UHFFFAOYSA-N | CIVKECGAWHNMMH-SYOLFDCTSA-N | DIKBKLULQCNWFE-UHFFFAOYSA-N | VDDAQBBXEZSNHH-UHFFFAOYSA-N | FHNSZOZVRKRZGQ-UHFFFAOYSA-N | IQKPCYQRKHJALH-UHFFFAOYSA-N | UMVYXLXQXUEFRV-UHFFFAOYSA-N | VSVKXOLIOSGVCJ-UHFFFAOYSA-L | VTHXEJIWTGATJW-UHFFFAOYSA-N | SEUCQUZIPWXOBH-UHFFFAOYSA-N | LRQIISNFNXZOAK-UHFFFAOYSA-J | WDSKYSABKOOQRK-UHFFFAOYSA-L | APAHXRGQWURMJR-UHFFFAOYSA-N | HREOABIJUTZHCI-UHFFFAOYSA-N | KVWZPQIVNKDUHM-UHFFFAOYSA-N | VOBMDCAGKGENRH-UHFFFAOYSA-N | UXMFHNKDQFFOOL-UHFFFAOYSA-N | OLNHBSNIVFVGGW-UHFFFAOYSA-N | NVRSOWPNPLTMAQ-UHFFFAOYSA-N | LAFORKIOPBPCNS-UHFFFAOYSA-N | OXJZEDNDPPJTJD-UHFFFAOYSA-N | VGGSQFUCUMXWEO-UHFFFAOYSA-N | LPGZPZDKTWWAEO-UHFFFAOYSA-N | AKBIZVWCXJQZLG-UHFFFAOYSA-J | LYJAGSWTKGGDOJ-UHFFFAOYSA-N | VNPMSJOKLISNOE-UHFFFAOYSA-N | LTGQENGTSNJDEH-UHFFFAOYSA-N | XLNXLMGKHNRSHN-UHFFFAOYSA-N | GSDRCAHUZXIGOX-UHFFFAOYSA-L | GUFOFKDUFACARE-UHFFFAOYSA-M | DKEHOOAKLFRDNY-UTZZRDIYSA-N | FPTIZLYXVNJBHP-UHFFFAOYSA-N | FZRZIQSGOOKBPC-UHFFFAOYSA-N | XLEGCVYSYKDRSA-UHFFFAOYSA-N | PLPJELUSDATAJG-UHFFFAOYSA-L | JISVROCKRBFEIQ-UHFFFAOYSA-N | GENAZHJYHPJKOC-UHFFFAOYSA-N | YYLXMOBNWLHUAR-BWRCCWPFSA-N | XYAPAZVKBADAFD-UHFFFAOYSA-N | GPUUZTOWDDTBBG-UHFFFAOYSA-N | XIOSRWXZKNQBOL-UHFFFAOYSA-N | ACIDS | CO2 | CHEMISTRY, PHYSICAL | ELECTROCHEMICAL REDUCTION | CATHODE | ENGINEERING, CHEMICAL | ALKENES | CARBON-DIOXIDE | SURFACES | Olefins | Butadiene | Catalysts | Formic acid | Density functionals | Atoms | Organic acids | or physical chemistry | Catalysis | Chemical Sciences | Theoretical and
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Journal of Chemical & Engineering Data, ISSN 0021-9568, 12/2018, Volume 63, Issue 12, pp. 4632 - 4648
This work reports densities, speeds of sound, and viscosities of binary mixtures of n-alkylcyclohexanes (propyl- to dodecylcyclohexane) in n-hexadecane as a... 
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2014, ISBN 9783527671236, Volume 9783527334902, xxii, 543 pages
This comprehensive reference and handbook covers in depth all major aspects of the use of N-heterocyclic carbene-complexes in organic synthesis: from the... 
Carbenes (Methylene compounds) | Synthesis | Heterocyclic compounds | Organometallic compounds | Heterocyclic chemistry | Transition metals
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