Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mingcai Fan"'
Autor:
Haiying Cui, Mingcai Fan, Yunbo Wang, Xiaochong Zhang, Wanling Xu, Yanan Li, Wenzheng Song, Jian-Ying Ma, Wei Sun
Publikováno v:
Plant and Soil. 482:7-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3380e3c8f488719f746590479ad8355
https://doi.org/10.1007/s11104-022-05670-4
https://doi.org/10.1007/s11104-022-05670-4
Publikováno v:
Plant Growth Regulation. 98:91-102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02eda7548ddaeea28b5ed8dc8ed1503a
https://doi.org/10.1007/s10725-022-00835-8
https://doi.org/10.1007/s10725-022-00835-8
Publikováno v:
Agricultural and Forest Meteorology. 330:109316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe528f35b734d6b4360f656733fc298d
https://doi.org/10.1016/j.agrformet.2023.109316
https://doi.org/10.1016/j.agrformet.2023.109316
Publikováno v:
Bulletin of the Chemical Society of Japan. 72:1571-1574
A variety of naphthopyrone hydroperoxides as novel photochemical DNA cleavers were synthesized and evaluated. Their photochemical DNA-cleaving abilities depend on skeleton arrangement of the naphthopyrone core and are much more efficient than those o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9985641c90c02ddf2c78a2bd768a81f
https://doi.org/10.1246/bcsj.72.1571
https://doi.org/10.1246/bcsj.72.1571
Publikováno v:
Tetrahedron. 53:13329-13338
Three angular furonaphthopyrones 4, 9, 12 were regioselectively synthesized starting from 2,7-naphthalenediol in three steps, respectively. An easy separation of Pechmann condensation products 1 and 2 of 2, 7-naphthalenediol with ethyl acetoacetate w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4436fed3571863a4b8de9a01ca4ce48e
https://doi.org/10.1016/s0040-4020(97)00845-4
https://doi.org/10.1016/s0040-4020(97)00845-4
Publikováno v:
ChemInform. 29
Three angular furonaphthopyrones 4, 9, 12 were regioselectively synthesized starting from 2,7-naphthalenediol in three steps, respectively. An easy separation of Pechmann condensation products 1 and 2 of 2, 7-naphthalenediol with ethyl acetoacetate w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e78c6ce038612253f0af4caaaf55bc04
https://doi.org/10.1002/chin.199805131
https://doi.org/10.1002/chin.199805131
Publikováno v:
ChemInform. 30
The efficient synthesis of several novel DNA-intercalating furonaphthopyrone derivatives with improved water solubility or photophysical properties are described. As expected, all new compounds can efficiently intercalate into DNA with higher or comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa328e1e2422423e8bcb94d31206b7fb
https://doi.org/10.1002/chin.199948143
https://doi.org/10.1002/chin.199948143
Publikováno v:
Monatshefte fuer Chemie/Chemical Monthly. 130:1109
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88b81a5e954a7ee36d9713771bca7b4b
https://doi.org/10.1007/s007060050270
https://doi.org/10.1007/s007060050270
Publikováno v:
Scopus-Elsevier
The efficient synthesis of several novel DNA-intercalating furonaphthopyrone derivatives with improved water solubility or photophysical properties are described. As expected, all new compounds can efficiently intercalate into DNA with higher or comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9e22b7fba5f6e6f8b2391f5e39b657e
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033425846&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033425846&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
3H-1,8,9-Trimethylthieno[3′,2′:6,7]naphtho[2,1-b]pyran-3-one, a potential photobiological agent, was synthesized in six steps starting from commercially available 2,7-naphthalenediol. The key step involved is a Newman–Kwart rearrangement of nap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8795d81de9a65783a5bd67bc6421a540
http://www.scopus.com/inward/record.url?eid=2-s2.0-0041192936&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0041192936&partnerID=MN8TOARS