An article Design and synthesis of chiral hyperbranched polymers containing cinchona squaramide moieties and their catalytic activity in the asymmetric Michael addition reaction WOS:000491683200053 published article about DENDRIMERS; ORGANOCATALYSTS; MOLECULES; CORE in [Chhanda, Sadia Afrin; Itsuno, Shinichi] Toyohashi Univ Technol, Dept Appl Chem & Life Sci, Toyohashi, Aichi 4418580, Japan in 2019, Cited 39. Category: thiomorpholine. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8
Chiral hyperbranched polymers (HBP) containing cinchona alkaloids were synthesized using a Mizoroki-Heck (MH) coupling polymerization reaction between a cinchona squaramide dimer and tri- or tetrasubstituted aromatic iodides. This is a new type of polymeric chiral organocatalyst. We found that the as-obtained chiral HBPs show excellent catalytic activity in the asymmetric Michael reaction. Almost perfect enantioselectivity (>99% ee) was achieved in the reaction of beta-ketoester and trans-beta-nitrostyrene. The three-dimensional network structure of the chiral HBPs is structurally robust and can be reused for further reaction without any loss in their catalytic activity. (C) 2019 Elsevier Inc. All rights reserved.
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,Thiomorpholine | C4H9NS – PubChem