Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Hai-Shan Jin"'
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b14febf31256d4be91d8d95c7467457
https://doi.org/10.1002/chem.202300467
https://doi.org/10.1002/chem.202300467
Publikováno v:
The Journal of Organic Chemistry. 87:5795-5803
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e46a81670f24d1de791f9b1b08ba8af6
https://doi.org/10.1021/acs.joc.2c00122
https://doi.org/10.1021/acs.joc.2c00122
Publikováno v:
Organic Letters. 23:5952-5957
The Rh(III)-catalyzed dual directing group assisted C-H activation/annulation of 3-arylisoxazolones with propargyl alcohols has been developed, which expands the application scope of isoxazolones in organic synthesis. This protocol also worked well w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f0566bedd311e5b8dbee81d38f45fed
https://doi.org/10.1021/acs.orglett.1c02049
https://doi.org/10.1021/acs.orglett.1c02049
Publikováno v:
Organic Chemistry Frontiers. 8:6350-6355
The first Ru(II)-catalyzed cascade C–H activation/annulation reactions of N-aryl-pyrazolidinones with sulfoxonium ylides for the synthesis of cinnoline-fused pyrazolidinones are reported. This transformation proceeds smoothly under operationally si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::654fbd351edfe52a75289d24773c5652
https://doi.org/10.1039/d1qo01001h
https://doi.org/10.1039/d1qo01001h
Publikováno v:
Organic Letters. 22:7358-7362
An unusual [2 + 3] cycloaddition of isatin azomethine imines (AIs) and in situ generated azaoxyallyl cations has been developed. It is the first example where AIs serve as the [C,O] 2-atom synthon in organic synthesis. This work not only reveals a ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::494b6a3a9bb504dedd2d61dfe2ef62c7
https://doi.org/10.1021/acs.orglett.0c02705
https://doi.org/10.1021/acs.orglett.0c02705
Publikováno v:
European Journal of Organic Chemistry. 2020:4988-4994
A simple method involving DBN‐mediated spirocyclopropanation of para‐quinone methides with 3‐chlorooxindoles is reported, providing a novel class of bis‐spiro compounds in short reaction times under mild conditions. Twenty‐four examples of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dda8d95636f32635c2906905950bb88
https://doi.org/10.1002/ejoc.202000830
https://doi.org/10.1002/ejoc.202000830
Autor:
Hai-Shan Jin, Yan Gu, Guangdi Wang, Jie-Huan Zhang, Li-Ming Zhao, Madhusoodanan Mottamal, Shanchun Guo
Publikováno v:
Future Med Chem
Aim: Histone deacetylase (HDAC) is an attractive target for antitumor therapy. Therefore, the development of novel HDAC inhibitors is warranted. Materials & methods: A series of HDAC inhibitors based on N-hydroxycinnamamide fragment was designed as t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f7766c752c05259a18cf1c9d397a20
https://doi.org/10.4155/fmc-2018-0587
https://doi.org/10.4155/fmc-2018-0587
Publikováno v:
Advanced Synthesis & Catalysis. 361:4811-4816
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4eeeec6f4dec33cebe938d5fdd10bb4
https://doi.org/10.1002/adsc.201900842
https://doi.org/10.1002/adsc.201900842
Publikováno v:
European Journal of Organic Chemistry. 2018:4787-4794
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9ee2ae9bb7aab895784d5d7eda0a2a8
https://doi.org/10.1002/ejoc.201800881
https://doi.org/10.1002/ejoc.201800881
Publikováno v:
Chemical communications (Cambridge, England). 55(71)
A novel cross 1,3-dipolar cycloaddition between azomethine imines with in situ generated nitrile oxides has been developed. This is the first example of employing a reaction partner containing two heteroatoms in the [3+3] cycloaddition involving azom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed399a955ab02f51bb89508626fd3f9a
https://pubmed.ncbi.nlm.nih.gov/31418760
https://pubmed.ncbi.nlm.nih.gov/31418760