Recently I am researching about CATALYZED ASYMMETRIC HYDROGENATION; METHODOLOGY COOPERATIVE CATALYSIS; COMPLEX RUPHOX-RU; C-H AMINATION; BORROWING HYDROGEN; ENANTIOSELECTIVE SYNTHESIS; DIASTEREOSELECTIVE SYNTHESIS; SECONDARY ALCOHOLS; N-ALKYLATION; KETONES, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21773145]; Projects for the Academic Leaders and Academic Backbones, Shaanxi Normal University [16QNGG008]; 111 projectMinistry of Education, China – 111 Project [B14041]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Xu, RR; Wang, K; Liu, HY; Tang, WJ; Sun, HM; Xue, D; Xiao, JL; Wang, C. The CAS is 177-11-7. Through research, I have a further understanding and discovery of 1,4-Dioxa-8-azaspiro[4.5]decane. Safety of 1,4-Dioxa-8-azaspiro[4.5]decane
A ruthenium-catalyzed formal anti-Markovnikov hydroamination of allylic alcohols for the synthesis of chiral gamma-amino alcohols is presented. Proceeding via an asymmetric hydrogen-borrowing process, the catalysis allows racemic secondary allylic alcohols to react with various amines, affording enantiomerically enriched chiral gamma-amino alcohols with broad substrate scope and excellent enantioselectivities (68 examples, up to >99 %ee).
Safety of 1,4-Dioxa-8-azaspiro[4.5]decane. Bye, fridends, I hope you can learn more about C7H13NO2, If you have any questions, you can browse other blog as well. See you lster.
Reference：
Piperidine – Wikipedia,
Piperidine | C5H7510N – PubChem