Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Shuzhong He"'
Publikováno v:
Frontiers in Plant Science, Vol 13 (2022)
The medicinal plants were wildly library of natural products in drug discovery. The most active molecules with seven-membered rings skeleton represent a challenge for construction. A stereoselectivity (4 + 3) cycloadditions between allenyl ethers and
Externí odkaz:
https://doaj.org/article/6a2cda23316142e7a437483a9c99684a
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
Haedoxans are a series of sesquilignan natural products isolated from the traditional insecticidal plant Phryma leptostachya. Given their significant insecticidal activity, haedoxans and related analogs have been considered as potential agents for pl
Externí odkaz:
https://doaj.org/article/8465785186114c8fa16e54e1caa9323d
Publikováno v:
Journal of Heterocyclic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::741506c4f24c849b2c506df37d2d7b3c
https://doi.org/10.1002/jhet.4660
https://doi.org/10.1002/jhet.4660
Autor:
Waygen Thor, Weijian Ye, Yuen Kit Cheng, Bo Wang, Chi-Sing Lee, Shuzhong He, Lantian Sun, Xuefeng Liang
Publikováno v:
Organic Chemistry Frontiers. 7:840-845
A method for synthesising cyclopenta[b]pyran-2-ones through direct (3 + 2) cycloaddition between 2-pyrones and vinyl cyclopropanes is described. In the presence of Pd2(dba)3/dppe in toluene, a series of 2-pyrones undergo chemoselective (3 + 2) cycloa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::888e5ba298acf8119f2cdf22edfb7247
https://doi.org/10.1039/d0qo00049c
https://doi.org/10.1039/d0qo00049c
Autor:
Xian Huang, Min Yang, Xiangyu Feng, Waygen Thor, Chi Sing Lee, Yuen Kit Cheng, Shuzhong He, Liangliang Kang
Publikováno v:
Organic Chemistry Frontiers. 7:255-260
(4 + 3) cycloadditions between allenyl ethers and furans are described. The reaction features an in situ formation of oxygen-stabilized oxyallyls via epoxidations of allenyl ethers in the presence of H2PO4−. The multiple interactions between the ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfdfe1fa9460c4403f09a7c5c4e7d203
https://doi.org/10.1039/c9qo01349k
https://doi.org/10.1039/c9qo01349k
Publikováno v:
Organic Chemistry Frontiers. 7:2243-2246
A concise synthesis of the tetracyclic skeleton of palhinine alkaloids is described. The approach features a bifunctional Lewis acid promoted Diels–Alder/carbocyclization cascade for the rapid construction of the isotwistane (tricyclo[4.3.1.03,7]de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56ecde51d15f29b2233a4cf1e1e1ce11
https://doi.org/10.1039/d0qo00554a
https://doi.org/10.1039/d0qo00554a
Autor:
Yunyun Li, Xiang Zhou, Shu-Ming Li, Yuping Zhang, Chun-Mao Yuan, Shuzhong He, Zaichang Yang, Song Yang, Kang Zhou
Publikováno v:
Journal of agricultural and food chemistry. 70(5)
Prenylated chalcones are found mainly in plants and exhibit diverse biological and pharmacological activities. Some of these compounds are components of food and dietary supplements with significant health benefits. In plants, they are derived from c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a4611421a4045b01c53d7c0b01ff547
https://pubmed.ncbi.nlm.nih.gov/35089022
https://pubmed.ncbi.nlm.nih.gov/35089022
Publikováno v:
Frontiers in Plant Science; 12/21/2022, Vol. 13, p1-10, 10p
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
Haedoxans are a series of sesquilignan natural products isolated from the traditional insecticidal plant Phryma leptostachya. Given their significant insecticidal activity, haedoxans and related analogs have been considered as potential agents for pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::954f6de024cb05ebad1f954f2bdf8af6
https://www.frontiersin.org/article/10.3389/fchem.2020.00460/full
https://www.frontiersin.org/article/10.3389/fchem.2020.00460/full
Publikováno v:
European Journal of Organic Chemistry. 2018:196-208
A small focus library of basiliolides including basiliolide A₁, basiliolide A₂, basiliolide C and their structural analogues have been prepared for the structure-activity relationship study. The synthesis features a cyclopropanation/ring-opening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5587376fa2d24e2aa0b72204e4fd355f
https://doi.org/10.1002/ejoc.201701211
https://doi.org/10.1002/ejoc.201701211