Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Lizuo, Wu"'
Publikováno v:
Chemical Communications. 58:3485-3488
Here, a novel method for the stereoselective synthesis of alkynyl cyclopropanes, by the silver-catalyzed alkynylcyclopropanation of alkenes using alkynyl N-nosylhydrazones as alkynyl carbene precursors, is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c809f33a3da92d50fcb1409117530636
https://doi.org/10.1039/d2cc00099g
https://doi.org/10.1039/d2cc00099g
Autor:
Bing Xu, Sanliang Li, Zhan-Ming Zhang, Yu Liu, Lujia Zhou, Danting Ji, Lizuo Wu, Junliang Zhang
Publikováno v:
Angewandte Chemie International Edition. 59:2769-2775
Sonogashira-type cross-couplings are one of the most significant alkynylations in organic chemistry. One of the first palladium-catalyzed intramolecular Heck/Sonogashira reactions of alkenes with terminal alkynes is now reported. With this method, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77684c0e2a74c585e9c4f4ad044daabf
https://doi.org/10.1002/anie.201913367
https://doi.org/10.1002/anie.201913367
Autor:
Yongquan, Ning, Qingmin, Song, Paramasivam, Sivaguru, Lizuo, Wu, Edward A, Anderson, Xihe, Bi
Publikováno v:
Organic letters. 24(2)
Here we report a silver-catalyzed alkynyl carbene insertion into β-ketocarbonyls using alkynyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9c59c28ed00ba87cf5e4753128d7f3d
https://pubmed.ncbi.nlm.nih.gov/34985288
https://pubmed.ncbi.nlm.nih.gov/34985288
Publikováno v:
Chemical science. 13(7)
A palladium catalyzed enantioselective Heck/borylation reaction of alkene-tethered aryl iodides was realized, delivering a variety of 2,3-dihydrobenzofuranyl boronic esters in high yield with excellent enantioselectivity. Asymmetric synthesis of chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb35cbbfe75e9bf92ca0be812d5359a0
https://pubmed.ncbi.nlm.nih.gov/35308863
https://pubmed.ncbi.nlm.nih.gov/35308863
Autor:
Lujia Zhou, Sanliang Li, Bing Xu, Danting Ji, Lizuo Wu, Yu Liu, Zhan‐Ming Zhang, Junliang Zhang
Publikováno v:
Angewandte Chemie. 132:2791-2797
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::489ce1fbd4a02153bbf33347827b0796
https://doi.org/10.1002/ange.201913367
https://doi.org/10.1002/ange.201913367
Autor:
Lujia Zhou, Yu Liu, Zhan-Ming Zhang, Lizuo Wu, Danting Ji, Junliang Zhang, Bing Xu, Zhiming Li
Publikováno v:
Journal of the American Chemical Society. 141:8110-8115
A highly enantioselective palladium-catalyzed iodine atom transfer cycloisomerization of unactivated alkenes has been developed. This represents the first example of highly enantioselective carboiodination of olefin-tethered aryl iodides, which provi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce1355347ba722f59328a605a794b87a
https://doi.org/10.1021/jacs.9b04332
https://doi.org/10.1021/jacs.9b04332
Publikováno v:
Organic Letters. 21:3018-3022
The highly exo- and enantioselective gold-catalyzed tandem heterocyclization/[4 + 3] cycloaddition of 2-(1-alkynyl)-2-alken-1-ones and 1,3-diphenylisobenzofuran was implemented by utilizing Ming-Phos, which provides a facile access to chiral seven-me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2446089272e15a9a0c7a96969f90151b
https://doi.org/10.1021/acs.orglett.9b00537
https://doi.org/10.1021/acs.orglett.9b00537
Publikováno v:
SSRN Electronic Journal.
Heck-type C-H bond activation of unactivated alkenes has emerged as a powerful strategy for the construction of synthetically valuable spirocycles over past 30 years, however, the development of asymmetric version has lagged largely behind. Herein we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7142227bab1213a253b37d9089f0da2
https://doi.org/10.2139/ssrn.3936039
https://doi.org/10.2139/ssrn.3936039
Autor:
Yuanqi Wu, Yanyan Qian, Zhan-Ming Zhang, Lujia Zhou, Junliang Zhang, Lizuo Wu, Yu Liu, Bing Xu
Publikováno v:
Angewandte Chemie International Edition. 57:10373-10377
The first example of highly enantioselective intramolecular hydroarylation of allyl aryl ethers was realized by palladium-catalyzed reductive heck reactions utilizing a new chiral sulfinamide phosphine ligand (N-Me-XuPhos). N-Me-XuPhos can be easily
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b18c14c0fdf5028f22cad249e9b489e
https://doi.org/10.1002/anie.201806372
https://doi.org/10.1002/anie.201806372
Autor:
Yuanqi Wu, Yu Liu, Yanyan Qian, Bing Xu, Zhan-Ming Zhang, Junliang Zhang, Lujia Zhou, Lizuo Wu
Publikováno v:
Angewandte Chemie (International ed. in English). 58(41)
A highly enantioselective dicarbofunctionalization of unactivated alkenes was implemented by a Pd-catalyzed asymmetric tandem Heck/Suzuki coupling reaction. This reaction represents the first example of a highly enantioselective intramolecular cycliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6784e17d6fbfc6efc3af0e7824eeb64f
https://pubmed.ncbi.nlm.nih.gov/31420928
https://pubmed.ncbi.nlm.nih.gov/31420928