the CAMS Innovation Fund for Medical Sciences (CIFMS,No.2021-I2M-1-026);the National Key R & D Program of China (No.2018YFE0111400);the NIH Research Project Grant Program (No.R01 EB025892);the National Natural Science Foundation of China (the Training Program of the Major Research Plan,No.91853120);the National Major Scientific and Technological Special Project of China (Nos.2018ZX09711001-005 and 2018ZX09711001-013);the State Key Laboratory of Bioactive Substance and Function of Natural Medicines,Institute of Materia Medica;the Biomedical High Performance Computing Platform,Chinese Academy of Medical Sciences,the Chinese Academy of Medical Sciences;Peking Union Medical College for funding and support
This study presents an unexpected finding that the cis isomer of β-thio-Asp exhibits higher ligation ac-tivity than the trans isomer.This discovery sheds light on the intricate nature of native chemical ligation and ...
the support from the Fudan University;supported by National Natural Science Foundation of China (Nos. 21890722 and 21950410519);National Natural Science Foundation of Tianjin (No. 19JCYBJC20100)
Oxygen ligation is envisioned to provide a stable and distinctive coordination environment to the strongly oxophilic rare-earth metals. However, the well-defined dialkyl complexes bearing oxyanion ancillary ligand had...
The highly regio-and stereoselective hydroborations of unactivated internal alkynes with diboron compound catalyzed by Cu(OTf)2 with spiro(phosphoamidite) as ligand in the presence of Cs2CO3 in water was developed...
A reaction of benzylic alcohols with alkenes has been developed in the presence of bis(trifluoromethane)sulfonimide for the synthesis of trisubstituted alkenes and indane derivatives with high stereoselectivity.In g...
the National Natural Science Foundation of China(No.20672095);CAS Academician Foundation of Zhejiang Province for financial support
A regio- and stereo-selective synthesis of multi-substituted 3-pyrrolines has been developed. The multi-substituted 3-pyrrolines were synthesized in good yields by 1,3-dipolar cycloaddition of methyl 2-(phenylselanyl...
Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.
D-mannitol through oxidation of its diacetonide gave aldehyde which condensed with PhTi(Oipr)3 stercoselechvely to yield (2R,3R) and (2R,3S) in the ratio of 9: 1. The 1,2-acetonide was transformed to 2,3-aeetonide ...