In 2019.0 ORG LETT published article about ALKENYLBORONIC ACIDS; ALPHA,BETA-UNSATURATED KETONES; STEREOSELECTIVE-SYNTHESIS; 1,4-ADDITION REACTION; ALKYNYLATION; ARYL; TRIFLUOROMETHYLATION; ALKENYLATION; CONSTRUCTION; RATIONALE in [Chai, Guo-Li; Sun, A-Qiang; Wang, Juan; Deng, Wei-Qiao; Wong, Henry N. C.; Chang, Junbiao] Henan Normal Univ, Sch Chem & Chem Engn, Henan Key Lab Organ Funct Mol & Drug Innovat, Xinxiang 453007, Henan, Peoples R China; [Zhai, Dong; Deng, Wei-Qiao] Shandong Univ, Inst Mol Sci & Engn, Qingdao 266237, Shandong, Peoples R China; [Wong, Henry N. C.] Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai Hong Kong Joint Lab Chem Synth, 345 Lingling Rd, Shanghai 200032, Peoples R China in 2019.0, Cited 51.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 100-19-6
(S)-2,15-Br-2-DHTP-catalyzed asymmetric conjugate addition of boronic acids to beta-trifluoromethyl alpha,beta-unsaturated ketones and enones was studied. The reaction afforded the corresponding Michael addition products in moderate to high yields with excellent enantioselectivities (up to 99:1 er). This catalytic system features mild reaction conditions, high efficiency, and tolerance to heteroarylboronic acids.
Welcome to talk about 100-19-6, If you have any questions, you can contact Chai, GL; Sun, AQ; Zhai, D; Wang, J; Deng, WQ; Wong, HNC; Chang, JB or send Email.. Recommanded Product: 100-19-6
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem