Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Longzhi, Zhu"'
Autor:
Dingzhong Li, Wensheng Zhang, Dr. Longzhi Zhu, Prof. Dr. Shuang‐Feng Yin, Prof. Dr. Nobuaki Kambe, Prof. Dr. Renhua Qiu
Publikováno v:
ChemistryOpen, Vol 11, Iss 5, Pp n/a-n/a (2022)
Abstract An efficient hydrazine substitution of p‐nitro‐aryl fluorides with hydrazine hydrates catalyzed by FeO(OH)@C nanoparticles is described. This hydrazine substitutions of p‐nitro‐aryl fluorides bearing electron‐withdrawing groups pro
Externí odkaz:
https://doaj.org/article/da9fa761793c461c9a6ad7f0578485a3
Autor:
Biquan Xiong, Chonghao Shi, Weifeng Xu, Yu Liu, Longzhi Zhu, Ke‐Wen Tang, Shuang‐Feng Yin, Wai‐Yeung Wong
Publikováno v:
Advanced Synthesis & Catalysis. 364:4392-4401
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::102de164cf9dce3ad07a3d70afeb82e8
https://doi.org/10.1002/adsc.202201055
https://doi.org/10.1002/adsc.202201055
Autor:
Biquan Xiong, Lulu Si, Longzhi Zhu, Rong Wu, Yu Liu, Weifeng Xu, Fan Zhang, Ke‐Wen Tang, Wai‐Yeung Wong
Publikováno v:
Chemistry – An Asian Journal. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85830b2ba3df9a932d13ec789fbfaf2e
https://doi.org/10.1002/asia.202201156
https://doi.org/10.1002/asia.202201156
Autor:
Biquan, Xiong, Lulu, Si, Longzhi, Zhu, Rong, Wu, Yu, Liu, Weifeng, Xu, Fan, Zhang, Ke-Wen, Tang, Wai-Yeung, Wong
Publikováno v:
Chemistry, an Asian journal.
A mild and efficient Zn(II)-catalyzed regioselective 1,6-hydroarylation of para-quinone methides (p-QMs) with electron-rich arenes protocol is reported. A variety of electron-rich arenes and para-quinone methides are well tolerated under mild conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f5b1272814c0e90bf5f66f249f3b324
https://pubmed.ncbi.nlm.nih.gov/36507597
https://pubmed.ncbi.nlm.nih.gov/36507597
Publikováno v:
Organic Letters. 23:5317-5322
A general and effective palladium-catalyzed cross-coupling of organostibines with styrenes to give (E)-olefins was disclosed. By the use of an organostibine reagent, this method can produce unsymmetric (E)-1,2-diarylethylenes and (1E,3E)-1,4-diarylbu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18811f7610df4077148469ea52871983
https://doi.org/10.1021/acs.orglett.1c01532
https://doi.org/10.1021/acs.orglett.1c01532
Publikováno v:
Organic Letters. 23:2514-2520
A simple and efficient methodology for the synthesis of large sterically hindered triarylamines in a single step was developed. A direct N,N-diarylation of 8-aminoquinoline with sterically hindered...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93a9dd746bcf6d02619c65ac25a40a92
https://doi.org/10.1021/acs.orglett.1c00463
https://doi.org/10.1021/acs.orglett.1c00463
Autor:
Fan Cao, Lulu Si, Shipan Xu, Longzhi Zhu, Yu Liu, Weifeng Xu, Ke-Wen Tang, Biquan Xiong, Wai-Yeung Wong
Publikováno v:
Tetrahedron Letters. 111:154207
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3392bd99c915b400afffd2deffac2508
https://doi.org/10.1016/j.tetlet.2022.154207
https://doi.org/10.1016/j.tetlet.2022.154207
Publikováno v:
The Journal of Organic Chemistry. 84:5635-5644
The reaction of trifluoroacetyl amides with Grignard reagent for the substitution of CF3 group with various alkyl or aryl groups is described. A variety of aryl, quinolin-8-yl, and (hetero)alkyl functional groups as well as F, Cl, and Br atoms are we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c718c4208ce20fa6f4ac8fcfe6763552
https://doi.org/10.1021/acs.joc.9b00583
https://doi.org/10.1021/acs.joc.9b00583
Publikováno v:
Organic letters. 23(14)
A general and effective palladium-catalyzed cross-coupling of organostibines with styrenes to give (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eefa02f6cf2fe86720658586d7ed11f3
https://pubmed.ncbi.nlm.nih.gov/34096311
https://pubmed.ncbi.nlm.nih.gov/34096311