Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ning‐Yuan Yang"'
Autor:
Yu‐Feng Zhang, Jia‐Huan Wang, Ning‐Yuan Yang, Zheng Chen, Li‐Lei Wang, Qiang‐Shuai Gu, Zhong‐Liang Li, Xin‐Yuan Liu
Publikováno v:
Angewandte Chemie International Edition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b40b972a6f522e1d2e97a341b6dd708
https://doi.org/10.1002/anie.202302983
https://doi.org/10.1002/anie.202302983
Autor:
Fu-Li Wang, Chang-Jiang Yang, Ji-Ren Liu, Ning-Yuan Yang, Xiao-Yang Dong, Ruo-Qi Jiang, Xiao-Yong Chang, Zhong-Liang Li, Guo-Xiong Xu, Dai-Lei Yuan, Yu-Shuai Zhang, Qiang-Shuai Gu, Xin Hong, Xin-Yuan Liu
Publikováno v:
Nature Chemistry. 14:949-957
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41afcb87f694977a499087c5ae852d09
https://doi.org/10.1038/s41557-022-00954-9
https://doi.org/10.1038/s41557-022-00954-9
Autor:
Qiang-Shuai Gu, Cheng Luan, Li-Lei Wang, Fu-Li Wang, Xin-Yuan Liu, Juan Liu, Ning-Yuan Yang, Jiang-Tao Cheng, Zhong-Liang Li, Yu-Feng Zhang, Xiao-Yang Dong
Publikováno v:
Journal of the American Chemical Society. 143:15413-15419
α-Chiral alkyl primary amines are virtually universal synthetic precursors for all other α-chiral N-containing compounds ubiquitous in biological, pharmaceutical, and material sciences. The enantioselective amination of common alkyl halides with am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c9f8038f866214c44eafecd43571d0d
https://doi.org/10.1021/jacs.1c07726
https://doi.org/10.1021/jacs.1c07726
Autor:
Wen-Yue Tang, Yong-Feng Cheng, Qiang-Shuai Gu, Xin-Yuan Liu, Ji-Jun Chen, Zhong-Liang Li, Jun-Qian Bian, Zhuang Li, Xian-Yan Cheng, Ning-Yuan Yang
Publikováno v:
Organometallics. 40:2215-2219
A cobalt-catalyzed enantioconvergent radical Negishi C(sp3)–C(sp2) cross-coupling of racemic benzyl chlorides with arylzinc reagents has been developed in good yield with moderate enantioselectivit...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bc84f28b5d4c1f7e16fe6d54cb0b4a2
https://doi.org/10.1021/acs.organomet.1c00190
https://doi.org/10.1021/acs.organomet.1c00190
Autor:
Zhong-Liang Li, Xin-Yuan Liu, Qiang-Shuai Gu, Tian-Ya Zhan, Cheng Luan, Jiao Yu, Liu Ye, Guo-Qiang Chen, Ning-Yuan Yang, Jiang-Tao Cheng
Publikováno v:
Organic Letters. 23:1945-1949
We have described a copper-catalyzed radical 1,2-carbotrifluoromethylselenolation of alkenes using the readily available alkyl halides and (Me4N)SeCF3 salt. Critical to the success is the use of a proline-based N,N,P-ligand to enhance the reducing ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8397cd9d63dd5449703a02378204803
https://doi.org/10.1021/acs.orglett.1c00436
https://doi.org/10.1021/acs.orglett.1c00436
Autor:
Fu-Li, Wang, Chang-Jiang, Yang, Ji-Ren, Liu, Ning-Yuan, Yang, Xiao-Yang, Dong, Ruo-Qi, Jiang, Xiao-Yong, Chang, Zhong-Liang, Li, Guo-Xiong, Xu, Dai-Lei, Yuan, Yu-Shuai, Zhang, Qiang-Shuai, Gu, Xin, Hong, Xin-Yuan, Liu
Publikováno v:
Nature chemistry. 14(8)
In contrast with the well-established enantioconvergent radical C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::80e97dbaad50882c9c377ce14d7a70fc
https://pubmed.ncbi.nlm.nih.gov/35618768
https://pubmed.ncbi.nlm.nih.gov/35618768
Autor:
Yu-Feng Zhang, Qiang-Shuai Gu, Liu Ye, Tian-Ya Zhan, Xin-Yuan Liu, Ning-Yuan Yang, Xiao-Yang Dong, Fu-Li Wang, Jiang-Tao Cheng, Ji-Jun Chen, Zhong-Liang Li
Publikováno v:
Journal of the American Chemical Society. 142(20)
A copper-catalyzed intermolecular three-component asymmetric radical 1,2-carboalkynylation of alkenes has been developed, providing straightforward access to diverse chiral alkynes from readily available alkyl halides and terminal alkynes. The utiliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b9f4252d715c4208d29023f3764d94d
https://pubmed.ncbi.nlm.nih.gov/32338510
https://pubmed.ncbi.nlm.nih.gov/32338510
Publikováno v:
Angewandte Chemie. 128:15324-15328
A novel radical 1,2-formylfunctionalization of alkenes involving 1,2(4,5)-formyl migration triggered by addition of various carbon- and heteroatom-centered radicals to alkenes has been developed for the first time, thus providing straightforward acce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86cb76430548d045dc05e8fbe613144
https://doi.org/10.1002/ange.201608198
https://doi.org/10.1002/ange.201608198
Publikováno v:
Chemical Communications. 52:9052-9055
An unprecedented and efficient organic base-catalysed highly chemoselective carbo- and oxytrifluoromethylation of unactivated alkenes with Togni's reagent was developed. The switchable chemoselectivity was tuned by simply changing the organic base ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7773ca0605cdf2153c54d249c5e2e7cd
https://doi.org/10.1039/c6cc00364h
https://doi.org/10.1039/c6cc00364h
Publikováno v:
Angewandte Chemie. 127:4113-4117
An unprecedented phosphine-catalyzed remote β-CH functionalization of amine derivatives triggered by trifluoromethylation of an alkene with Togni's reagent was disclosed. This reaction proceeded through the highly selective and concomitant activa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49653cf6130d47a29730c0ba2561dee6
https://doi.org/10.1002/ange.201412310
https://doi.org/10.1002/ange.201412310