Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ze-Shui Liu"'
Autor:
Bo Ding, Qilin Xue, Han Wei, Jiangwei Chen, Ze-Shui Liu, Hong-Gang Cheng, Hengjiang Cong, Jianting Tang, Qianghui Zhou
Publikováno v:
Chemical Science; 6/7/2024, Vol. 15 Issue 21, p7975-7981, 7p
Autor:
Chenggui Wu, Ze-Shui Liu, Yong Shang, Chang Liu, Shuang Deng, Hong-Gang Cheng, Hengjiang Cong, Yinchun Jiao, Qianghui Zhou
Publikováno v:
Chinese Journal of Chemistry; Apr2024, Vol. 42 Issue 7, p699-704, 6p
Publikováno v:
ACS Catalysis. 13:2968-2980
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fb785359c773404dbac9bcf12b5896a
https://doi.org/10.1021/acscatal.2c06310
https://doi.org/10.1021/acscatal.2c06310
Autor:
Yinchun Jiao, Hengjiang Cong, Chenggui Wu, Hong-Gang Cheng, Jinxiang Ye, Shuang Deng, Qianwen Gao, Qianghui Zhou, Yu Hua, Lisha Li, Chang Liu, Ze-Shui Liu
Publikováno v:
Journal of the American Chemical Society. 143:7253-7260
Herein, we report a modular and convergent strategy for the assembly of atropisomeric o-terphenyls with 1,2-diaxes via palladium/chiral norbornene cooperative catalysis and axial-to-axial diastereoinduction. Readily available aryl iodides, 2,6-substi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::218eac8ae2891546663a686f978af463
https://doi.org/10.1021/jacs.1c02405
https://doi.org/10.1021/jacs.1c02405
Autor:
Qianwen Gao, Yuanyuan Ma, Yong Shang, Hong-Gang Cheng, Yu Hua, Qianghui Zhou, Hua Tang, Ze-Shui Liu
Publikováno v:
Nature Catalysis. 3:727-733
Axially chiral biaryls are common structural motifs in functional materials, bioactive natural products, pharmaceuticals and chiral catalysts/ligands. As such, efficient preparation of these privileged scaffolds is an important endeavour in organic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ecad72222ff58e7cac4311459ecb626
https://doi.org/10.1038/s41929-020-0494-1
https://doi.org/10.1038/s41929-020-0494-1
Publikováno v:
Synthesis. 52:834-846
A cooperative catalytic system involving a Pd/XPhos complex and inexpensive 5-norbornene-2-carbonitrile that enables the use of alkyl tosylates as alkylating reagents in the Catellani reaction has been developed. This mild, scalable protocol is compa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a00220d0904f74e20e25eb203ccc6cd4
https://doi.org/10.1055/s-0039-1690801
https://doi.org/10.1055/s-0039-1690801
Publikováno v:
Tetrahedron. 75:1774-1780
Mediators play a central role in Catellani-type reactions. Herein we reported the discovery of inexpensive 5-norbornene-2-carboxylic acid (N4) as a general catalytic mediator (20 mol%) to facilitate ortho C–H activation and the following C–C bond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5292c7089ef000a9c41816b1c1da17f
https://doi.org/10.1016/j.tet.2019.01.033
https://doi.org/10.1016/j.tet.2019.01.033
Autor:
Hengjiang Cong, Chenggui Wu, Shuang Deng, Hong-Gang Cheng, Yong Shang, Qianghui Zhou, Chang Liu, Ze-Shui Liu, Yinchun Jiao
Publikováno v:
Angewandte Chemie (International ed. in English). 60(32)
Herein we report an asymmetric two-component vinylogous Catellani reaction for the construction of C-N axial chirality through a palladium/chiral norbornene cooperative catalysis and an axial-to-axial chirality transfer process. Various partially aro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82740a6206b7dcfe01b1e2967708b84a
https://pubmed.ncbi.nlm.nih.gov/34033193
https://pubmed.ncbi.nlm.nih.gov/34033193
Autor:
Qianwen, Gao, Chenggui, Wu, Shuang, Deng, Lisha, Li, Ze-Shui, Liu, Yu, Hua, Jinxiang, Ye, Chang, Liu, Hong-Gang, Cheng, Hengjiang, Cong, Yinchun, Jiao, Qianghui, Zhou
Publikováno v:
Journal of the American Chemical Society. 143(19)
Herein, we report a modular and convergent strategy for the assembly of atropisomeric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1cd35c1e2ccd0a986e67a0cd9bf33200
https://pubmed.ncbi.nlm.nih.gov/33961421
https://pubmed.ncbi.nlm.nih.gov/33961421
Kinetic Resolution of Tertiary Benzyl Alcohols via Palladium/Chiral Norbornene Cooperative Catalysis
Publikováno v:
Angewandte Chemie (International ed. in English). 60(23)
Herein we report a highly enantioselective kinetic resolution of tertiary benzyl alcohols via palladium/chiral norbornene cooperative catalysis. With simple aryl iodides as the resolution reagent, a wide range of readily available racemic tertiary be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab5e9406eb743f96e8a3d254ca3823a6
https://pubmed.ncbi.nlm.nih.gov/33783116
https://pubmed.ncbi.nlm.nih.gov/33783116