Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Xinglin Ye"'
Publikováno v:
Royal Society Open Science, Vol 8, Iss 1 (2021)
Novel daidzein napsylates (DD4 and DD5) were synthesized by microwave irradiation, according to structural modification of daidzein (DAI) using the principle of pharmacokinetic transformation. The pharmacological properties of DD4 and DD5 were evalua
Externí odkaz:
https://doaj.org/article/dd10c4a386394bfdae5713a55fc55947
Publikováno v:
Synthesis. 54:788-796
A series of 2-(hetero)aryl-4-phosphorylated quinazolines was successfully synthesized in moderate to excellent yields via a palladium-catalyzed C–O/P–H cross-coupling reaction of 4-(tosyloxy)quinazolines with H-phosphonates and phosphine oxides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c7b6a163e2cf8424965792f8fd09f54
https://doi.org/10.1055/a-1647-5978
https://doi.org/10.1055/a-1647-5978
Autor:
Huanan Huang, Lingxiu Liu, Jianguo Wang, Ying Zhou, Huanan Hu, Xinglin Ye, Guochang Liu, Zhixiong Xu, Han Xu, Wen Yang, Yawei Wang, You Peng, Pinghua Yang, Jianqi Sun, Ping Yan, Xiaohua Cao, Ben Zhong Tang
Publikováno v:
Chemical science. 13(11)
Polycyclic aromatic hydrocarbons (PAHs) with boron-nitrogen (BN) moieties have attracted tremendous interest due to their intriguing electronic and optoelectronic properties. However, most of the BN-fused π-systems reported to date are difficult to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a62185614fe40617a5e2451be8f3593
https://pubmed.ncbi.nlm.nih.gov/35414886
https://pubmed.ncbi.nlm.nih.gov/35414886
Publikováno v:
Canadian Journal of Chemistry. 97:682-689
Using cheap, readily available, and economic active MnO2 as an oxidant, a series of 2,4-disubstituted quinazoline-3-oxides were synthesized in good to excellent yields by oxidation of the corresponding 1,2-dihydroquinazoline-3-oxides under mild condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68bb944c98a0596cdf17b5025b2ce53e
https://doi.org/10.1139/cjc-2018-0521
https://doi.org/10.1139/cjc-2018-0521
Publikováno v:
Royal Society Open Science, Vol 8, Iss 1 (2021)
Royal Society Open Science
Royal Society Open Science
Novel daidzein napsylates (DD4 and DD5) were synthesized by microwave irradiation, according to structural modification of daidzein (DAI) using the principle of pharmacokinetic transformation. The pharmacological properties of DD4 and DD5 were evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::669e99558344e6123030d24a23e3386a
https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.201475
https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.201475
Novel daidzein napsylates (DD4 and DD5) were synthesized by microwave irradiation, according to structural modification of daidzein (DAI) using the principle of pharmacokinetic transformation. The pharmacological properties of DD4 and DD5 were evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14fd5656f4462e3fc3d7179dea77db34
Novel daidzein napsylates (DD4 and DD5) were synthesized by microwave irradiation, according to structural modification of daidzein (DAI) using the principle of pharmacokinetic transformation. The pharmacological properties of DD4 and DD5 were evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c7be180bed81fbe13c236e0bc934b99
Publikováno v:
Synthesis. 48:3976-3984
An efficient route to 4-substituted quinazolines by arylation or alkylation of quinazolinones under mild conditions is described. 4-Tosyloxyquinazolines were obtained through the reaction of quinazolinones and p-methylbenzenesulfonyl chloride in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::136bff4b512e78748d46d8ca611ca4e7
https://doi.org/10.1055/s-0035-1562504
https://doi.org/10.1055/s-0035-1562504
Publikováno v:
Journal of Heterocyclic Chemistry. 53:1956-1962
A series of 2,4-diarylquinazolines have been successfully synthesized via the Ni-catalyzed cross-coupling reaction of quinazoline-4-tosylates and aryl Grignard reagents, which provided alternative straightforward approaches for the introduction of ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6042c2d112bc47ef93452ed5b28d6f26
https://doi.org/10.1002/jhet.2513
https://doi.org/10.1002/jhet.2513
Publikováno v:
Synthetic Communications. 41:3728-3734
Trisubstituted 1,3-dienes can be stereoselectively synthesized in one pot under mild conditions, in good yields, by hydromagnesiation of alkylarylacetylenes, followed by the palladium-catalyzed cross-coupling with alkenyl iodides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38d1f2427e5abc2b9d06c40c7c89cb08
https://doi.org/10.1080/00397911.2010.520400
https://doi.org/10.1080/00397911.2010.520400