Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Xi-Chao Wang"'
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
Transition metal-catalyzed reactions of silacyclobutanes to access structurally diverse organosilicon compounds have attracted attention in recent years. Here, the authors show nickel-catalysed, ligand-controlled chemodivergent reactions of these com
Externí odkaz:
https://doaj.org/article/d55a66170de04d9a9a9c734822e9ca6c
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Bis-silylated alkenes offer the advantage of two functional handles with distinguished reactivity for downstream functionalization. Here, the authors report a nickel-catalyzed bis-silylation of internal alkynes to versatile silylated alkene intermedi
Externí odkaz:
https://doaj.org/article/d98163b8a0ff4e948f20431981c2b554
Autor:
Cheng-Wei Ju, Xi-Chao Wang, Bo Li, Qiushi Ma, Yuhao Shi, Jinyu Zhang, Yuzhi Xu, Qian Peng, Dongbing Zhao
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 11/14/2023, Vol. 120 Issue 46, p1-10, 52p
Autor:
Xi-Chao Wang1 dongbing.chem@nankai.edu.cn, Hao-Ran Wang2 xxfang@nankai.edu.cn, Xiufang Xu2, Dongbing Zhao1
Publikováno v:
European Journal of Organic Chemistry. 6/7/2021, Vol. 2021 Issue 21, p3039-3042. 4p.
Publikováno v:
European Journal of Organic Chemistry. 2021:3039-3042
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::781bff995fce72a88a4c77bb1f4b28e6
https://doi.org/10.1002/ejoc.202100535
https://doi.org/10.1002/ejoc.202100535
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Nature Communications
Nature Communications
1,2-Bis-silyl alkenes have exciting synthetic potential for programmable sequential synthesis via manipulation of the two vicinal silyl groups. Transition metal-catalyzed bis-silylation of alkynes with disilanes is the most straightforward strategy t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d80b91ea93b37b987fc7ee676e3378f
https://doaj.org/article/d98163b8a0ff4e948f20431981c2b554
https://doaj.org/article/d98163b8a0ff4e948f20431981c2b554
Autor:
Hao-jie Zhang, Peng-peng Ding, Xiang-sheng Zhang, Xi-chao Wang, Di-wen Sun, Qing-ao Bu, Xiao-qiang Li
Publikováno v:
International immunopharmacology. 113
Plasma cell mastitis (PCM) and granulomatous mastitis (GM) are common inflammatory nonbacterial mastitis (NBM). However, the pathogenesis of NBM is still unclear.Methods. In this study, we statistically analyzed the pathological features of PCM and G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d885560c18a5a833bef99076329187fb
https://pubmed.ncbi.nlm.nih.gov/36252469
https://pubmed.ncbi.nlm.nih.gov/36252469
Autor:
Jie Yang, Xiao‐Ming Zhang, Fu‐Min Zhang, Shao‐Hua Wang, Yong‐Qiang Tu, Zhen Li, Xi‐Chao Wang, Hong Wang
Publikováno v:
Angewandte Chemie. 132:8549-8553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca6bfa62fff0ca1a5c3dec45f4976be
https://doi.org/10.1002/ange.202001100
https://doi.org/10.1002/ange.202001100
Investigations of the sila-8-membered ring fused biaryls are of important significance for the discovery of new drug lead compounds. However, such compounds are still unknown due to the synthetic challenge. Herein we describe the chemo- and regio-sel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5a8441e1f6879fe020faebff22f7d9
https://doi.org/10.26434/chemrxiv.14510718
https://doi.org/10.26434/chemrxiv.14510718
Autor:
Fu-Min Zhang, Xiao-Ming Zhang, Hong Wang, Zhen Li, Yong-Qiang Tu, Xi-Chao Wang, Jie Yang, Shao-Hua Wang
Publikováno v:
Angewandte Chemie (International ed. in English). 59(22)
An enantioselective aldehyde α-alkylation/semipinacol rearrangement was achieved through organo-SOMO catalysis. The catalytically generated enamine radical cation serves as a carbon radical electrophile that can stereoselectively add to the alkene o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::628dbe2a765724ae24ae06909f21f956
https://pubmed.ncbi.nlm.nih.gov/32124524
https://pubmed.ncbi.nlm.nih.gov/32124524