supported by the National Key Research and Development Program of China (2022YFB4101800);the National Natural Science Foundation of China (22231002);the Guangdong Basic and Applied Basic Research Foundation (2024B1515040027)。
Indole is a promising heteroarene in many natural products and pharmaceuticals;therefore, various synthetic methods for indole functionalizations have arisen in recent years. Herein, we report a Pd-catalyzed deoxygena...
Glycosides are essential structural motifs present in an array of important medicines,materials,and natural products[1].Nevertheless,the chemo-and stereoselective construction of the glycosidic linkage is a long-stand...
supported by the National Key R&D Program of China(2021YFA1500100);the National Natural Science Foundation of China(21821002,92256303,22171278);Shanghai Science and Technology Committee(23ZR1482400);the Natural Science Foundation of Ningbo(2023J034)。
Transition metal-catalyzed olefination of aryl C-H bond is a powerful tool for the synthesis of alkenes. While the Pd-catalyzed oxidative C-H olefination of arenes, also known as Fujiwara-Moritani reaction, has been e...
supported by the National Key Research and Development Program of China(2021YFA0804900);the Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang(2022R01007);Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism。
Palladium-catalyzed allylic alkylation enabled by ketone umpolung via Pudovik addition/[1,2]-phospha-Brook rearrangement with phosphites has been developed.The protocol offers a straightforward method for the synthesi...
supported by the National Natural Science Foundation of China(21831005,21991112,22171183);the Science and Technology Commission of Shanghai Municipality(19JC1430100)。
In contrast to the stereocontrol of the stereocenter at the allyl unit,the asymmetric induction of prochiral nucleophiles remains a challenge in Pd-catalyzed asymmetric allylic substitutions due to the remote distance...
supported by the National Natural Science Foundation of China(22171224,21971204);the Innovation Capability Support Program of Shaanxi Province(2020TD-022);the Fund of Education Department of Shaanxi Provincial Government(22JP082)。
Hydrocarbonylation of conjugated dienes is one of the most promising yet challenging methods for the synthesis of carbonyl compounds.Herein,we reported the development of an unprecedented palladium-catalyzed branched ...
supported by the National Natural Science Foundation of China (22188101, 21831007, 21971231, 21772184)。
The discovery of novel catalysis modes to generate a significant increase in structural complexity from readily available reactants is a fundamental goal in modern organic synthesis.Here,we report a photoinduced palla...
supported by the National Natural Science Foundation of China(21801225);the Science Foundation for Young Teachers(2019td02);High-level Talent Research Start-up Project(2018TP018)of Wuyi University;the Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme(2019);the Department of Education of Guangdong Province(2020KCXTD036)。
Carbonylation,one of the most powerful approaches to the preparation of carbonylated compounds,has received significant attention from researchers active in various fields.Indeed,impressive progress has been made on t...
supported by the National Natural Science Foundation of China (21831007)。
Chiral homoallylic vicinal diols are found in many bioactive compounds and are among the most versatile functional groups in organic chemistry. Here, we describe an asymmetric carbonyl allylation of aldehydes with all...
the National Natural Science Foundation of China(21901239,21532006);the Strategic Priority Program of Chinese Academy of Sciences(XDB17020300,QYZDJ-SSW-SLH035)。
The developments of hydrogen sources stand at the forefront of asymmetric reduction. In contrast to the well-studied alcohols as hydrogen sources via β-hydride elimination, the direct utilization of the proton of alc...