supported by the National Key R&D Program of China (2017YFA0204704);the National Natural Science Foundation of China (21602105);the General Program of Chongqing Natural Science(cstc2020jcyj-msxmX0712);Ningbo Natural Science Foundation (202003N4063);the Natural Science Foundation of Jiangsu Province (BK20221309)
Axially chiral molecules have been widely used in inorganic,material and medicinal chemistry.Compared with well-established N-heterocyclic carbene(NHC)-catalyzed asymmetric construction of centrally chiral molecules,N...
support of the National Natural Science Foundation(21971094).
The first N-heterocyclic carbene-catalyzed enantioselective dearomatizing annulation of benzoxazoleswith α,β-unsaturated aldehydes has been achieved. The reaction was found to be compatible with a widerange of benzo...
Junta de Castilla y León(Projects:FEDER-VA115P17,and VA149G18)for financial support;the Laboratory of Instrumental Techniques(LTI)Research Facilities,Universidad de Valladolid;Junta de Castilla y León for a predoctoral fellowship(EDU/556/2019);grant PID2020-113147GA-I00 funded by MCIN/AEI/10.13039;by the Fundación Salamanca City of Culture and Knowledge(programme for attracting scientific talent to Salamanca);Grant No.EDU/601/2020(Junta de Castilla y Leon and European Social Fund).
Chiral pyrazolones with a spirocyclic centre at the C4-position are widely found in a large family of medically relevant compounds.In recent years,organocatalysis,particularly that performed with quiral N-heterocyclic...
supported by the National Natural Science Foundation of China (No.21572053);Opening Project of Zhejiang Provincial Preponderant and Characteristic Subject of Key University (Traditional Chinese Pharmacology),Zhejiang Chinese Medical University (No.ZYAOX2018029)。
An unprecedented chiral secondary amine-catalyzed [3+3] annulation of isatin N,N’-cyclic azomethine imines with α,β-unsaturated aldehydes was developed.This strategy allowed the construction of structurally novel s...
Financial support for this work by the National Natural Science Foundation of China(No.81202403);West China HospitalChengdu Science and Technology Department Translational Medicine Innovation Foundation(No.ZH13039)
A simple and efficient cascade Michael/cyclization reaction of 3-aminoindolin-2-ones with enones/enals was identified for the synthesis of potentially biologically active 3',4'-dihydrospiro[pyrrol-3,2'-oxindoles], ...
the financial support from the National Science Foun-dation (CHE-1057569,W. W.);the China 111 Project (B07023,J. L. and W. W.);the National Natural Science Foundation of China (20972051,X. Y.-H.);the Science and Technology Commission of Shanghai Mu-nicipality (08430703900 & 08431901800,X. Y.-H.)
A mild and highly efficient amine-catalyzed, IBX-mediated oxidation of aldehydes to (E) selective a, β-unsamrated aldehydes has been achieved in good yields. The process features a new oxidation of enamines to imin...