Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Yan-Kai Liu"'
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 16615-16625 (2018)
Externí odkaz:
https://doaj.org/article/efa03ef955d946489ce435a1448a6375
Publikováno v:
Advances in Materials Science and Engineering, Vol 2021 (2021)
Permeation grouting is widely used in grouting engineering because of its low grouting pressure and minor disturbance to the stratum. However, influenced by the complex properties of sand layer and slurry, an accurate prediction of the groutability o
Externí odkaz:
https://doaj.org/article/310bc7acb47a405da55580f5bb7cf5e9
Publikováno v:
Organic Letters. 25:1706-1710
Publikováno v:
Organic Letters.
Publikováno v:
Organic letters. 24(50)
The organocatalytic enantioselective Michael addition of functionalized prochiral cyclic hemiacetals and nitroolefins has been developed under cooperative enamine and hydrogen bond catalysis. The obtained chiral hemiacetal intermediates could be used
Publikováno v:
Organic Letters. 23:6515-6519
An efficient aminocatalytic enantioselective double-activation strategy has been developed that combines several different aminocatalytic modes in a cascade process, such as iminium ion, vinylogous iminium ion, trienamine, and dienamine activations.
Autor:
Yan-Kai Liu, Zhihao You
Publikováno v:
Organic letters. 24(34)
Based on the intramolecular E1cB elimination, a novel [4 + 2] cyclization was designed and successfully applied to the asymmetric synthesis of polycyclic compounds which contained both chromane and spirooxindole moieties. In the reaction, regardless
Publikováno v:
2022 International Joint Conference on Neural Networks (IJCNN).
Publikováno v:
Organic Chemistry Frontiers. 8:4217-4223
An organocatalytic enantioselective conjugate addition-initiated reaction sequence of 2-hydroxycinnamaldehydes with various functionalized nitroalkanes has been described. The combination of iminium catalysis and thiourea hydrogen-bonding catalysis w
Publikováno v:
Organic Chemistry Frontiers. 8:6309-6316
A Bronsted acid-catalyzed cascade acyclic N,O-hemiaminal formation/oxa-Michael reaction is developed for the synthesis of cis-2,6-disubstituted tetrahydropyrans bearing an exo amide group, that is, cyclic N,O-aminals. By using TsOH, various different