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Application In Synthesis of Benzophenone. Welcome to talk about 119-61-9, If you have any questions, you can contact Zhou, XB; Zhang, GY; Huang, RB; Huang, HM or send Email.

Authors Zhou, XB; Zhang, GY; Huang, RB; Huang, HM in AMER CHEMICAL SOC published article about CHIRAL DIPHOSPHINE LIGANDS; ALKYL-HALIDES; ENANTIOSELECTIVE SYNTHESIS; ASYMMETRIC-SYNTHESIS; ARYL BROMIDES; COMPLEXES; HYDROGENOLYSIS; HYDROGENATION; ALDEHYDES; ELIMINATION in [Zhou, Xibing; Huang, Renbin; Huang, Hanmin] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China; [Zhou, Xibing; Huang, Renbin; Huang, Hanmin] Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China; [Zhang, Guoying; Huang, Hanmin] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China; [Huang, Hanmin] Chinese Acad Sci, Ctr Excellence Mol Synth, Hefei 230026, Peoples R China in 2021.0, Cited 70.0. Application In Synthesis of Benzophenone. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Catalytic carbon-carbon bond formation building on reductive coupling is a powerful method for the preparation of organic compounds. The identification of environmentally benign reductants is key for establishing an efficient reductive coupling reaction. Herein an efficient strategy enabling H-2 as the sole reductant for the palladium-catalyzed allyl-allyl reductive coupling reaction is described. A wide range of allylamines and allylic alcohols as well as allylic ethers proceed smoothly to deliver the C-C coupling products under 1 atm of H-2. Kinetic studies suggested that the dinuclear palladium species was involved in the catalytic cycle.

Application In Synthesis of Benzophenone. Welcome to talk about 119-61-9, If you have any questions, you can contact Zhou, XB; Zhang, GY; Huang, RB; Huang, HM or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem