科学略号の検索サイト「なのに〜る」

 
p-toluenesulfonyl (Ts)
 

(1) A more sustainable and highly practicable synthesis of aliphatic isocyanides (Green Chem. 2020, 22, 933−941; 10.1039/C9GC04070F) Ts

(2) Employing TosMIC as a C1N1 “Two-Atom Synthon” in Imidazole Synthesis by Neighboring Group Assistance Strategy (Org. Lett. 2020, 22, 140−144; 10.1021/acs.orglett.9b04060) Ts

(3) Ferrocenoyl conjugates of hydroxyl group containing side chain amino acids: Synthesis, electrochemical study and reactivity toward electrophiles (J. Organomet. Chem. 2020, 906, 121056−; https://doi.org/10.1016/j.jorganchem.2019.121056) Ts

(4) I2/CuCl2-promoted one-pot three-component synthesis of aliphatic or aromatic substituted 1,2,3-thiadiazoles (Chem. Commun. 2019, 55, 8134−8137; 10.1039/C9CC04254G) Ts, Tos, tosyl, SCN, K, Me

(5) Synthesis of the Hexasaccharide Fragment of Landomycin A Using a Mild, Reagent-Controlled Approach (Org. Lett. 2019, 21, 3674−3677; 10.1021/acs.orglett.9b01118) Ts, Tos, tosyl, TsC, TosCl, TsCl

 
 
 
thymidylate synthase (TS)
 

(1) Convenient Synthesis and Anticancer Activity of Methyl 2-[3-(3-Phenyl-quinoxalin-2-ylsulfanyl)propanamido]alkanoates and N-Alkyl 3-((3-Phenyl-quinoxalin-2-yl)sulfanyl)propanamides (ACS Omega 2019, 4, 18555−18566; 10.1021/acsomega.9b02320) TS

(2) Inter-Active Site Communication Mediated by the Dimer Interface Î-Sheet in the Half-the-Sites Enzyme, Thymidylate Synthase (Biochemistry 2019, 58, 3302−3313; 10.1021/acs.biochem.9b00486) TS, MR, MD, CS, NMR, Cat

(3) Fuplatin: An Efficient and Low-Toxic Dual-Prodrug (J. Med. Chem. 2019, 62, 4543−4554; 10.1021/acs.jmedchem.9b00128) TS, FU, 5-FU, Efudex, FUra, CP

(4) Mixed ligand ternary complexes of Co(II), Ni(II), Cu(II) and Zn(II) and their structural characterization, electrochemical, theoretical and biological studies (J. Mol. Struct. 2019, 1187, 108−120; https://doi.org/10.1016/j.molstruc.2019.03.031) TS, FMO, CV, CV, Ala, A, TC, H, EC, SP, SPy, SPl, MO, CP, DFT, SB, HDF, e-, HB, XRD, MS

(5) Synthesis and Structure–Activity Relationship Studies of Benzo[b][1,4]oxazin-3(4H)-one Analogues as Inhibitors of Mycobacterial Thymidylate Synthase X (ChemMedChem 2019, 14, 645−662; 10.1002/cmdc.201800739) TS, Mtb, TB, FDTS

 
 
 
transition structure (TS)
 

(1) Multireference Study of the H2COO (Criegee Intermediate) + O3 Addition: A Reaction of Possible Tropospheric Interest (J. Phys. Chem. A 2020, 124, 1112−1120; 10.1021/acs.jpca.9b11430) TS

(2) Tetragonal Mixed System Cs2CuCl4–xBrx Complemented by the Tetragonal Phase Realization of Cs2CuCl4 (Cryst. Growth Des. 2019, 19, 6627−6635; 10.1021/acs.cgd.9b01035) AF, TS

(3) Catalysis by Pure Graphene—From Supporting Actor to Protagonist through Shape Complementarity (J. Org. Chem. 2019, 84, 11343−11347; 10.1021/acs.joc.9b01909) TS, C, Cat

(4) Potential Energy Surfaces of HN(CH)SX:CO2 for X = F, Cl, NC, CN, CCH, and H: N···C Tetrel Bonds and O···S Chalcogen Bonds (J. Phys. Chem. A 2019, 123, 7270−7277; 10.1021/acs.jpca.9b04144) CC, BE, TS, PES, EOM, EOM-CC, CT, BDE, M

(5) A model study on the mechanism and kinetics for reactions of the hydrated electron with H3O+ and NH4+ ions (Chem. Phys. Lett. 2019, 731, 136604−; https://doi.org/10.1016/j.cplett.2019.136604) TS, HAT, H, QC, e-, DFT

 
 
 
transition state (TS)
 

(1) Design of Substrate Transmembrane Mimetics as Structural Probes for γ-Secretase (J. Am. Chem. Soc. 2020, 142, 3351−3355; 10.1021/jacs.9b13405) TMD, TSA, biol., TM, PR, TS

(2) Mode Specificity in the OH + HO2 → H2O + O2 Reaction: Enhancement of Reactivity by Exciting a Spectator Mode (J. Am. Chem. Soc. 2020, 142, 3331−3335; 10.1021/jacs.9b12467) H, R, TS

(3) DFT approach to the pathway of conformational changes of cellulose C6-hydroxymethyl group with simple cellotetraose model involving the mechanism of mercerization process (Chem. Phys. Lett. 2020, 742, 137154−; https://doi.org/10.1016/j.cplett.2020.137154) PES, H, TS

(4) Synthesis of Cyclobutane-Fused Tetracyclic Scaffolds via Visible-Light Photocatalysis for Building Molecular Complexity (J. Am. Chem. Soc. 2020, 142, 3094−3103; 10.1021/jacs.9b12129) PS, VLP, Ir, TS

(5) Understanding the chemistry of cation leaching in illite/water interfacial system using reactive molecular dynamics simulations and hydrothermal experiments (Acta Mater. 2020, 186, 564−574; https://doi.org/10.1016/j.actamat.2019.12.059) aq., Fe, est., K, TS

 
 
 
temperature-sensitive (ts)
 

(1) Intra-articular injection of indomethacin–methotrexate in situ hydrogel for the synergistic treatment of rheumatoid arthritis (J. Mater. Chem. B 2020, 8, 993−1007; 10.1039/C9TB01795J) ts

(2) Synthesis of Temperature/pH Dual-Stimuli-Response Multicompartmental Microcapsules via Pickering Emulsion for Preprogrammable Payload Release (ACS Appl. Mater. Interfaces 2020, 12, 4821−4832; 10.1021/acsami.9b20999) ts

(3) Streptavidin Homologues for Applications on Solid Surfaces at High Temperatures (Langmuir 2020, 36, 628−636; 10.1021/acs.langmuir.9b02339) ts

(4) A stably discrete 31-nuclearity silver(I) thiolate nanocluster luminescent thermometer supported by DMF auxiliary ligands (New J. Chem. 2020, 44, 663−667; 10.1039/C9NJ05076K) ts

(5) The Purple Flask: A Novel Reformulation of the Blue Bottle Reaction (J. Chem. Educ. 2020, 97, 159−161; 10.1021/acs.jchemed.9b00627) ts

 
 
 
through-space interaction (TS)
 

(1) Ultrafast Vibrational Energy Transfer through the Covalent Bond and Intra- and Intermolecular Hydrogen Bonds in a Supramolecular Dimer by Two-Dimensional Infrared Spectroscopy (J. Phys. Chem. B 2020, 124, 544−555; 10.1021/acs.jpcb.9b10431) TS

(2) Singlet Energy Transfer in Anthracene–Porphyrin Complexes: Mechanism, Geometry, and Implications for Intramolecular Photon Upconversion (J. Phys. Chem. B 2019, 123, 9934−9943; 10.1021/acs.jpcb.9b07991) TS

(3) Singlet Energy Transfer in Anthracene–Porphyrin Complexes: Mechanism, Geometry, and Implications for Intramolecular Photon Upconversion (J. Phys. Chem. B 2019, 123, 9934−9943; 10.1021/acs.jpcb.9b07991) TS

(4) Nonstationary Two-Dimensional Nuclear Magnetic Resonance: A Method for Studying Reaction Mechanisms in Situ (Anal. Chem. 2019, 91, 11306−11315; 10.1021/acs.analchem.9b02414) TS, MR, Bn, PhH, BZ, DL, PhMe, Ph2CH2, MRS, Nu, CS, TolH, NMR

(5) 1-Carbazolyl Spirobifluorene: Synthesis, Structural, Electrochemical, and Photophysical Properties (J. Phys. Chem. C 2019, 123, 19094−19104; 10.1021/acs.jpcc.9b02507) TS, OMO, FL, EC, MO, cbz, OLED, PhOLED, LE, HOMO, e-, LED, BB

 
 
 
total syntheses (TS)
 
 
 
 
total synthesis (TS)
 
 
 
February 21, 2020
ケイデンスを上げる。
February 21, 2020
青色光照射下での反応です。
J. Am. Chem. Soc. 2020, 142 (7), 3366−3370.
February 20, 2020
株主総会の日。
February 20, 2020
エノラートの幾何異性制御。
Org. Lett. 2020, 2 (3), 791−794.
February 19, 2020
氷点下5度割れ。
February 19, 2020
DBUで落とすのかと思ってました。
Chem. Lett. 2020, 49 (3), 252−253.
February 18, 2020
「呉カレーふりかけ」なるものを試した。
February 18, 2020
不斉反応です。
Org. Lett. 2020, 22 (3), 1135−1138.
よく読まれている記事をアーカイブ化しました。
August 22, 2019
ホウ素アタックが鍵です。
Chem. Commun. 2019, 55 (68), 10166−10169.
February 6, 2020
フマル酸とマレイン酸の覚え方。
Angew. Chem. Int. Ed. 2020, 59 (7), 2760−2763.
December 29, 2015
JavascriptとPerlを組み合わせ、アクセスランキングなどをWebに表示させたいときなどに使います。
June 28, 2017
AIGというと、一般的にはアメリカン・インターナショナル・グループ。
June 7, 2016
放電すると残量が増えていく!
January 27, 2020
開環メタセシス重合。
J. Am. Chem. Soc. 2020, 142 (3), 1186−1189.
July 31, 2019
Ir触媒下での反応。
Angew. Chem. Int. Ed. 2019, 58 (32), 11054−11057.
September 3, 2019
まとめました。羽化しないアゲハもいる。
March 11, 2016
分子ではないですよ。
August 8, 2019
まとめました。含BNπ共役系。
December 25, 2019
流れ流れてなが…
Org. Lett. 2019, 21 (24), 10094−10098.
May 29, 2016
あくまでもネタとしてお読みください。
January 1, 2020
2018年と比較すると興味深い傾向が
December 11, 2019
ご参考になれば
June 7, 2016
バッテリーを交換しても充電できないままだが何かが変だった話。
May 28, 2016
無理くりになりましたので、結果は予想通りに。
October 5, 2017
にゃー→まぉー→あぅー
読みたいけと読んでいない論文を、構造式を描きながら紹介します(2019年10〜12月)。
February 11, 2018
うん、やっぱりこうなるよね。
September 30, 2019
WordPress最後の記事。
November 22, 2016
何を習ったかを思い出せ。
December 26, 2019
部分日食見えず。
December 29, 2015
忘れないように書き留めておきました。
(c) Nanoniele, 2003-