supported by the National Natural Science Foundation of China (22071183);the Science and Technology Commission of Shanghai Municipality (19DZ2271500)。
Chiral phosphine-containing skeletons play a pivotal role in bioactive natural products, pharmaceuticals, chiral catalysts, and ligands. Despite considerable progress has been made in the synthesis of chiral phosphoru...
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...
Ministry of Science and Technology of China(2015CB856600);the National Natural Science Foundation of China(21672197,21602214);the Chinese Academy of Sciences(XDB20020000).
A highly regio-and enantioselective allylic C–H alkylation of 1,4-dienes with glycine Schiff bases has been established by chiral palladium-phosphoramidite catalysis. This reaction can proceed under mild conditions a...
During the past decade, there was increased interest in the functionalization of the allylic C-H bond of alkenes. As opposed to traditional Trost-Tsuji reactions, this strategy avoids the prefunctionalization of the a...
supported by the National Natural Science Foundation of China (Grant Nos. 20621091,20672048,and 20732002);the "111" program of Chinese Education Ministry
Construction of the polyaryl quaternary unit through a ZnBr2 catalyzed tandem coupling/semipinacol rearrangement participated by allylic cations was reported for the first time.
Supported by the National Natural Science Foundation of China (Grant No. 20772084)
The enantioselective O-allylic alkylation of acetophenone oxime with various Morita-Baylis-Hillman (MBH) carbonates has been accomplished by the catalysis of a commercially available cinchona alkaloid (DHQD)2PHAL. The...