support from the Natural Science Foundation of Guangxi(2023GXNSFDA026063);National Natural Science Foundation of China(22261036);High-level Innovation Team and Outstanding Scholar Program in Guangxi Colleges and Universities.
A regiodivergent synthesis of azetidines,5,6-dihydro-1,3-oxazines and 2,3-dihydro-1,4-oxazines has been achieved through palladium-catalyzed tandem allylic substitution reaction.This protocol provides a variety of het...
National Natural Science Foundation of China(No.22101133);Natural Science Foundation of Jiangsu Province(No.BK20200768)and Nanjing Forestry University are greatly acknowledged.
An efficiently catalytic method toward the synthesis of indolin-2-ones featuring an allylic derived C_(3)-quaternary stereocenter via an intramolecular Heck cyclization/Suzuki coupling of N-substituted-N-(2-bromopheny...
supported by the National Natural Science Foundation of China(Grants 21971080,21971079,21772051);This work was also supported by the 111 Project B17019.
Comprehensive Summary The conversion of CF3-alkenes to gem-difluoroalkenes using reductive cross-coupling strategy has received much attention in recent years,however,the use of green and readily available reducing sa...
the National Key R&D Program of China(2021YFA1500100);Youth Innovation Promotion Association CAS(2020448);NSFC(22171254 and 22188101);Anhui Provincial Natural Science Foundation(2108085MB58);USTC Research Funds of the DoubleFirst-Class Initiative(YD2060002024);Start-up Research Fund from University of Science and Technology of China(KY2060000216).
Comprehensive Summary Pd-catalyzed asymmetric allylic C—H functionalization has emerged as a powerful tool to access chiral,densely functionalized molecules from easily accessible alkenes,enabling the increase of the...
We are grateful for financial support from NSFC(Nos.21772069,21831007 and 21702077);the Natural Science Founda-tion of Jiangsu Province(No.BK20170227);Six Kinds of Talents Project of Jiangsu Province(No.SWYY-025).
of main observation and conclusion A new class of indole-based allylic donors have been designed and developed for palladium-catalyzed decarboxylative allylations.In addition,the first application of these indole-base...
We thank the National Natural Science Foundation of China (Nos. 21871145, 21672107 and 91856104) for financial support.
1.Introduction The past few decades have witnessed extensive studies on transition metal-catalyzed C-H bond activations and subsequent carbon-carbon and/or carbon-heteroatom bond formations because these methods provi...
The Nationa authors gratefully acknowledge the financial support from Natural Science Foundation of China (21625206, 21632009, 21372247, 21572258, 21572259, 21421002) and the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB20000000) and the Syngenta Ph.D. Fellowship (Y. Gu and C. Lu).
Highly regiodivergent copper-catalyzed allylic/propargylic difluoromethylation reactions by employing different ligands are described. When 5,6-dimethyl-1,10-phenanthroline was used as the ligand, exclusively α-diflu...
ein a Pd-catalyzed intramolecular allylation reaction of unprotected allylic alcohols was developed,and the reaction proceeded through a Pd(Ⅱ)-mediated allylic carbocation species formation,followed by a Friedel-Cr...
Two types of allylic trifluoromethylated compounds were synthesized by reacting alkynes with CF3CH2I using visible-light photocatalysis. Subtle differences in the catalytic system controlled the selectivity of iodotri...
Acknowledgement Financial support from National Natural Science Foundation of China (Nos. 21072100; 21121002; 21272119) is gratefully acknowledged.
in this work, the phosphine-catalyzed annulation reactions between modified allylic derivatives and polar 1,1-dicyano-1,3-dienes have been studied. In the catalysis of PPh3 (20 mol%), a [4 + 1 ] annulation reaction...