WordNet

(mechanics) the equal and opposite force that is produced when any force is applied to a body; "every action has an equal and opposite reaction"
a response that reveals a persons feelings or attitude; "he was pleased by the audiences reaction to his performance"; "John feared his mothers reaction when she saw the broken lamp"
a bodily process occurring due to the effect of some antecedent stimulus or agent; "a bad reaction to the medicine"; "his responses have slowed with age" (同)response
doing something in opposition to another way of doing it that you dont like; "his style of painting was a reaction against cubism"
an idea evoked by some experience; "his reaction to the news was to start planning what to do"
extreme conservatism in political or social matters; "the forces of reaction carried the election"

PrepTutorEJDIC

{名}(…に対する)『反応』《+『to』+『名』》 / 〈U〉(…に対する)(政治的・社会的な)『反動』,逆コース《+『against』+『名』》 / 〈U〉〈C〉化学反応,化学変化 / 〈U〉〈C〉(物理学で)反作用

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1. 急性輸血反応が疑われる患者に対するアプローチ approach to the patient with a suspected acute transfusion reaction
2. 薬物アレルギー：分類および臨床的特徴 drug allergy classification and clinical features
3. 分子標的剤およびその他の生物製剤を用いた癌治療による皮膚合併症 cutaneous complications of molecularly targeted therapy and other biologic agents used for cancer therapy
4. 全身化学療法に対する輸注反応 infusion reactions to systemic chemotherapy
5. 造影剤に対する即時型過敏反応：再発反応の予防 immediate hypersensitivity reactions to radiocontrast media prevention of recurrent reactions

Transformation of benzophenone-type UV filters by chlorine: Kinetics, products identification and toxicity assessments.

Li J1, Ma LY1, Xu L2.
Journal of hazardous materials.J Hazard Mater.2016 Jul 5;311:263-72. doi: 10.1016/j.jhazmat.2016.02.059. Epub 2016 Mar 4.
The present study focused on the kinetics, transformation pathways and toxicity of several benzophenone-type ultraviolet filters (BPs) during the water chlorination disinfection process. The transformation kinetics of the studied three BPs was found to be second-order reaction, which was dependent o
PMID 27035274

Nandi RK1, Ratsch F, Beaud R, Guillot R, Kouklovsky C, Vincent G.
Chemical communications (Cambridge, England).Chem Commun (Camb).2016 Apr 18;52(30):5328-31. doi: 10.1039/c6cc01654e. Epub 2016 Mar 23.
We report the FeCl3-mediated direct addition of electron-rich arenes to the C2-position of electrophilic N-Ac indoles under mild conditions (room temperature, air). No functional group is required on the arene nucleophile: one of its C-H bonds is added to the C2[double bond, length as m-dash]C3 doub
PMID 27005518

A Chiral Electrophilic Selenium Catalyst for Highly Enantioselective Oxidative Cyclization.

Kawamata Y1, Hashimoto T1, Maruoka K1.
Journal of the American Chemical Society.J Am Chem Soc.2016 Apr 15. [Epub ahead of print]
Chiral electrophilic selenium catalysts have been applied to catalytic asymmetric transformations of alkenes over the past two decades. However, highly enantioselective reactions with a broad substrate scope have not yet been developed. We report the first successful example of this reaction employi
PMID 27064419

Iron-Catalyzed Suzuki–Miyaura Coupling Reaction of Unactivated Alkyl Halides with Lithium Alkynylborates

, ,
Chemistry Letters advpub(0), 2015
… A Suzuki–Miyaura coupling reaction between unactivated alkyl halides and lithium alkynylborates was performed using an iron-bisphosphine catalyst. … The reaction shows high chemoselectivity and is applicable to a broad scope of substrates bearing electrophilic functional groups. …
NAID 130004868432

Use of In Situ Generated Nitrosocarbonyl Compounds in Catalytic Asymmetric α-Hydroxylation and α-Amination Reactions

,
Bulletin of the Chemical Society of Japan advpub(0), 2015
… However, the transient nature and incompatibility of the catalytic processes with their generation incarcerated their use mostly in hetero-Diels-Alder and ene reaction. … In this account we will summarize our effort to utilize the nitrosocarbonyl compounds as source of electrophilic oxygen and nitrogen in variety of asymmetric carbon-hetero-atom bond forming reactions. … The O- vs N-selectivity can be tuned by switching reaction conditions. …
NAID 130004801884

The Nickel(II)-Catalyzed Direct Benzylation, Allylation, Alkylation, and Methylation of C-H Bonds in Aromatic Amides Containing an 8-Aminoquinoline Moiety as the Directing Group

, ,
Bulletin of the Chemical Society of Japan advpub(0), 2015
… Direct alkylation via the cleavage of the ortho C-H bonds by a nickel-catalyzed reaction of aromatic amides containing an 8-aminoquinoline moiety as the directing group with alkyl halides is reported. … Various alkyl halides, including benzyl, allyl, alkyl, and methyl halides (or pseudo halides) participate as electrophilic coupling partners. … The reaction shows a high functional group compatibility. …
NAID 130004801859