- 関
- regioselective
English Journal
- Modification of the length and structure of the linker of N(6)-benzyladenosine modulates its selective antiviral activity against enterovirus 71.
- Drenichev MS1, Oslovsky VE1, Sun L2, Tijsma A2, Kurochkin NN1, Tararov VI1, Chizhov AO3, Neyts J2, Pannecouque C2, Leyssen P2, Mikhailov SN4.
- European journal of medicinal chemistry.Eur J Med Chem.2016 Mar 23;111:84-94. doi: 10.1016/j.ejmech.2016.01.036. Epub 2016 Jan 26.
- Very recently, we demonstrated that N(6)-isopentenyladenosine, a cytokinin nucleoside, exerts a potent and selective antiviral effect on the replication of human enterovirus 71. The present study is devoted to the structure optimization of another natural compound: N(6)-benzyladenosine. We mainly fo
- PMID 26854380
- Pyrone Diels-Alder Routes to Indolines and Hydroindolines: Syntheses of Gracilamine, Mesembrine, and Δ(7) -Mesembrenone.
- Gan P1, Smith MW2,1, Braffman NR2, Snyder SA3,4,5.
- Angewandte Chemie (International ed. in English).Angew Chem Int Ed Engl.2016 Mar 7;55(11):3625-30. doi: 10.1002/anie.201510520. Epub 2016 Feb 10.
- Although the Diels-Alder reaction has long been utilized for the preparation of numerous heterocycles, opportunities to extend its power remain. Herein, we detail a simple, modular, and robust approach that combines various amines regioselectively with 4,6-dichloropyrone to create substrates which,
- PMID 26865400
- Switching the cleavage sites in palladium on carbon-catalyzed carbon-carbon bond disconnection.
- Hattori T, Takakura R, Ichikawa T, Sawama Y, Monguchi Y, Sajiki H.
- The Journal of organic chemistry.J Org Chem.2016 Mar 4. [Epub ahead of print]
- We have demonstrated a palladium on carbon catalyzed approach to regioselectively alter the cleavage sites of the C-C bonds of cinnamaldehyde derivatives by the slight change of the reaction conditions in isopropanol under O2 atmosphere. Styrene derivatives could be selectively formed by the additio
- PMID 26944077
Japanese Journal
- Alteration of the substrate specificity of cytochrome P450 CYP199A2 by site-directed mutagenesis(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
- Furuya Toshiki,Shitashima Yoh,Kino Kuniki
- Journal of bioscience and bioengineering 119(1), 47-51, 2015-01
- … In whole-cell assays with p-methylbenzylalcohol and phenol as hydroxy aromatic substrates, the S247D mutant regioselectively oxidized these compounds to 1,4-benzenedimethanol and hydroquinone, respectively, although the wild-type enzyme exhibited no oxidation activity for these compounds. …
- NAID 110009892232
- DBU-promoted regioselective HBr-elimination of vicinal dibromides: effects of the adjacent oxygen and/or other heterofunctional groups
- Kutsumura Noriki,Toguchi Shohei,Iijima Masatoshi,Tanaka Osamu,Iwakura Izumi,Saito Takao
- Tetrahedron 70(43), 8004-8009, 2014-10
- … These HBr-eliminations proceeded more or less regioselectively, and all associated calculation results agreed with the experimental facts. …
- NAID 120005516380
- Regioselective Preparation of 4-Nitro-o-xylene Using Nitrogen Dioxide/Molecular Oxygen over Zeolite Catalysts. Remarkable Enhancement of para-Selectivity
- , , , ,
- Chemistry Letters 43(6), 817-819, 2014
- … In the presence of molecular oxygen and zeolite H-β with Si/Al2 = 500, o-xylene reacted regioselectively with liquid nitrogen dioxide at 35 °C to yield mononitro-o-xylenes as the main product, where the 4-nitro-o-xylene isomer predominated up to 89% and the 4-nitro-/3-nitro-o-xylene isomer ratio improved to 7.8. …
- NAID 130004868143
Related Links
- Adverb (comparative more regioselectively, superlative most regioselectively) In a regioselective manner With regard to regioselection
- regioselectively (comparative more regioselectively, superlative most regioselectively) In a regioselective manner With regard to regioselection Retrieved from "http://en.wiktionary.org/w/index.php?title=regioselectively&oldid=8437256 ...
★リンクテーブル★
[★]
- 英
- regioselective、regioselectively
- 関
- 位置選択性
[★]
- 関
- regioselectively、regioselectivity