Formula: C7H8N2O. Authors Laconsay, CJ; Seguin, TJ; Wheeler, SE in AMER CHEMICAL SOC published article about in [Laconsay, Croix J.; Seguin, Trevor J.; Wheeler, Steven E.] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA; [Wheeler, Steven E.] Univ Georgia, Dept Chem, Athens, GA 30602 USA in 2020, Cited 55. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6
Chiral phosphoric acids have received considerable attention because of their excellent performance in many asymmetric catalytic reactions. However, the full breadth of means by which the stereoselectivity of these catalysts can be tuned has not been fully elucidated. Herein, the origin of enantioselectivity in a catalytic asymmetric synthesis of 2,3-dihydroquinazolinones using SPINOL-derived chiral phosphoric acids (ACS Catal. 2013, 3, 2244) is explored using density functional theory computations. We show that the enantioselectivity of this reaction is determined during the intramolecular amine addition step of an organocascade sequence and is modulated by differential noncovalent interactions of the substrate with the aryl groups of the catalyst as well as CH center dot center dot center dot O and NH center dot center dot center dot O interactions with the phosphate core of the catalyst. Most notably, we demonstrate that the strength of these latter interactions is modulated by their position within the electrostatic environment created by the catalyst. This provides clear evidence of the ability to precisely control the selectivity of an organocatalyzed reaction through the tuning of electrostatic interactions.
Welcome to talk about 88-68-6, If you have any questions, you can contact Laconsay, CJ; Seguin, TJ; Wheeler, SE or send Email.. Formula: C7H8N2O
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem