Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Linghui Gu"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1591-1599 (2021)
The efficient copper-mediated oxidative C–H alkynylation of benzhydrazides was accomplished with terminal alkynes. Thus, a heteroaromatic removable N-2-pyridylhydrazide allowed for domino C–H/N–H functionalization. The approach featured remarka
Externí odkaz:
https://doaj.org/article/d62adeb0c15c48a494420bf1596aec97
Publikováno v:
Advanced Synthesis & Catalysis. 364:3881-3887
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::988015c4240e8428eff3c8cc8a0bd226
https://doi.org/10.1002/adsc.202200745
https://doi.org/10.1002/adsc.202200745
Publikováno v:
Asian Journal of Organic Chemistry. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17d23e22257e469f29965705ae26bec8
https://doi.org/10.1002/ajoc.202300024
https://doi.org/10.1002/ajoc.202300024
Publikováno v:
Chemical Communications. 58:7566-7569
An unprecedented electrochemical selenium-π-acid promoted hydration of internal alkynes bearing a phosphonate auxiliary was described. Thus, valuable (hetero)aryl and alkyl ketones could be accessed under mild, metal- and external oxidant-free condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df5362eea947f79de01f84cbb460509a
https://doi.org/10.1039/d2cc01901a
https://doi.org/10.1039/d2cc01901a
Publikováno v:
Organicbiomolecular chemistry. 21(1)
Herein, we report the rhodium-catalyzed tunable divergent synthesis of tetrasubstituted 1,3-enynes and alkynylated benzofurans via C−H alkenylation/DG migration and [3 + 2] annulation, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff869960594f94433c8304a1fb70739a
https://pubmed.ncbi.nlm.nih.gov/36465010
https://pubmed.ncbi.nlm.nih.gov/36465010
Autor:
Yangbin Lu, Siyu Liu, Xin Gong, Xiaoning Zhang, Fei Zhao, Hui Mao, Xiaowei Wu, Linghui Gu, Jin Qiao, Aiqiong Jia
Publikováno v:
Asian Journal of Organic Chemistry. 10:3308-3320
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9acce45a07ccfdd9aa18e294c369b9f9
https://doi.org/10.1002/ajoc.202100476
https://doi.org/10.1002/ajoc.202100476
Publikováno v:
ChemistrySelect. 6:8839-8842
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c786a3af7704c4e19be0a8355a0709d7
https://doi.org/10.1002/slct.202101676
https://doi.org/10.1002/slct.202101676
Publikováno v:
Food Research International. 168:112735
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28710fde6a522e6f50b5ed9fef2320d9
https://doi.org/10.1016/j.foodres.2023.112735
https://doi.org/10.1016/j.foodres.2023.112735
Publikováno v:
Organic Letters. 23:6200-6205
Herein, we report a highly efficient ruthenium-catalyzed peri-selective C(sp2)-H acylmethylation of 1-naphthols with α-carbonyl sulfoxonium ylides by utilizing hydroxyl as a weakly coordinating directing group. This new method imparts good reactivit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2588deb37373ee5a094b2d7591ea92c7
https://doi.org/10.1021/acs.orglett.1c01684
https://doi.org/10.1021/acs.orglett.1c01684
Publikováno v:
ChemCatChem. 13:1738-1742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1f0d848579e571316f981534f6ffe21
https://doi.org/10.1002/cctc.202002056
https://doi.org/10.1002/cctc.202002056