Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Xiang-Huan Shan"'
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
The synthesis of high value heterocycles from cheap starting materials remains challenging. Here, the authors develop a new strategy to realize practical and modular synthesis of N-H indoles and analogs from toluene and nitrile derivatives using natu
Externí odkaz:
https://doaj.org/article/563d47fb14df4979816cb875748aa53b
Autor:
Yiyao Ge, Jingjie Ge, Biao Huang, Xixi Wang, Guigao Liu, Xiang-Huan Shan, Lu Ma, Bo Chen, Guanghua Liu, Songmo Du, An Zhang, Hongfei Cheng, Qingbo Wa, Shiyao Lu, Lujiang Li, Qinbai Yun, Kuo Yuan, Qinxin Luo, Zhichuan J. Xu, Yonghua Du, Hua Zhang
Publikováno v:
Nano Research. 16:4650-4655
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b34c360c1e838417476aec5632093d4
https://doi.org/10.1007/s12274-022-5101-0
https://doi.org/10.1007/s12274-022-5101-0
Publikováno v:
Organic Chemistry Frontiers. 8:2981-2984
An efficient and practical transition metal free α-trideuteration of methylarenes was developed. This process proceeds via an inexpensive base, such as sodium hydroxide or potassium tert-butoxide, prompted deprotonation and reprotonation of methylar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1edbe54d54ab14881f43f5a146730b7
https://doi.org/10.1039/d1qo00265a
https://doi.org/10.1039/d1qo00265a
Publikováno v:
Organic Letters. 22:4553-4556
A transition-metal-free indole synthesis using radical coupling of 2-halotoluenes and imines via the later-stage C-N bond construction was reported for the first time. It includes an aminyl radical generation by C-H cleaving addition of 2-halotoluene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::829952800d188455ab2fd1ba9d3e5e1f
https://doi.org/10.1021/acs.orglett.0c01615
https://doi.org/10.1021/acs.orglett.0c01615
Publikováno v:
Chemical Communications. 56:4063-4066
In this work, CuSO4 is utilized as a practical redox catalyst for tandem dual annulation in the synthesis of indole-fused tetracyclic heteroacenes, which are important skeletons in both medicinal chemistry and materials chemistry. The preparation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b8e9a6a98f4c68e55cf234d0418eefc
https://doi.org/10.1039/d0cc01172j
https://doi.org/10.1039/d0cc01172j
Publikováno v:
Organic Letters. 22:357-360
A CuSO4-catalyzed tandem benzylic C–H insertion cyclization of toluene derivatives and isonitriles is described. The naturally abundant salt CuSO4 serves as a low-cost ligand-free redox catalyst. T...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec9eaf1418946d6586191f787d0d112c
https://doi.org/10.1021/acs.orglett.9b03751
https://doi.org/10.1021/acs.orglett.9b03751
Publikováno v:
Organic letters. 23(5)
An iron-catalyzed α,β-dehydrogenation of carbonyl compounds was developed. A broad spectrum of carbonyls or analogues, such as aldehyde, ketone, lactone, lactam, amine, and alcohol, could be converted to their α,β-unsaturated counterparts in a si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f861b2a743fc997078f871add536384f
https://pubmed.ncbi.nlm.nih.gov/33577342
https://pubmed.ncbi.nlm.nih.gov/33577342
Publikováno v:
Chemical communications (Cambridge, England). 56(29)
In this work, CuSO4 is utilized as a practical redox catalyst for tandem dual annulation in the synthesis of indole-fused tetracyclic heteroacenes, which are important skeletons in both medicinal chemistry and materials chemistry. The preparation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5c8a25541b0f9c374e85a9c0f011788
https://pubmed.ncbi.nlm.nih.gov/32162642
https://pubmed.ncbi.nlm.nih.gov/32162642
Publikováno v:
Organic Letters. 20:7898-7901
The first example of phenanthroline-tBuOK promoted intramolecular radical C–H arylation of N-(2-iodobenzyl)indoles without involvement of transition metals has been developed. A variety of substituted 6H-isoindolo [2, 1-a] indoles were prepared by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60db1e84bf46f8a03dd5736ec6289cf4
https://doi.org/10.1021/acs.orglett.8b03449
https://doi.org/10.1021/acs.orglett.8b03449
Publikováno v:
Organic letters. 22(2)
A CuSO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4aeddb59b80a6b8732af3cb3b65d272c
https://pubmed.ncbi.nlm.nih.gov/31887043
https://pubmed.ncbi.nlm.nih.gov/31887043