Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Guo-Li Huang"'
Publikováno v:
Chinese Journal of Chemistry. 40:2756-2762
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c1a416e9f882f0fa3655c03e55dc949
https://doi.org/10.1002/cjoc.202200407
https://doi.org/10.1002/cjoc.202200407
Publikováno v:
Green Chemistry. 24:6840-6844
A visible light-driven metal- and oxidant-free procedure for the decarboxylative alkylation of Baylis–Hillman acetates with N-(acyloxy)phthalimides to access trisubstituted alkyl acrylates under mild reaction conditions is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a035e2444bda112c41e3b118f427b87
https://doi.org/10.1039/d2gc02562k
https://doi.org/10.1039/d2gc02562k
Publikováno v:
New Journal of Chemistry. 46:10934-10939
An efficient procedure for p-toluenesulfonic acid-catalyzed iodination of isoquinolin-1(2H)-ones with N-iodosuccinimide under mild reaction conditions is reported. This methodology features scalable synthesis, wide substrate scope, and high functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f06a69751976fc39cd85feccc3afa81e
https://doi.org/10.1039/d2nj00159d
https://doi.org/10.1039/d2nj00159d
Publikováno v:
Asian Journal of Organic Chemistry. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ff10e950ea841a688f892fcd0e7a5fe
https://doi.org/10.1002/ajoc.202100694
https://doi.org/10.1002/ajoc.202100694
Autor:
Ming-yu Teng, Ai-hui Zhou, Peng-bin Si, Tao Han, Xiao-qing Liu, Guo-li Huang, Bo Liu, Jie Zhang
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98c7bf7d5e4fba258e02751c46328990
https://doi.org/10.2139/ssrn.4178957
https://doi.org/10.2139/ssrn.4178957
Autor:
Ai-hui Zhou, Tao Han, Peng-bin Si, Xiao-qing Liu, Ming-yu Teng, Guo-li Huang, Bo Liu, Qin Wang, Jie Zhang
Publikováno v:
Journal of Organometallic Chemistry. 985:122596
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1049d76013f79a5ebab9f19b9677b0b6
https://doi.org/10.1016/j.jorganchem.2022.122596
https://doi.org/10.1016/j.jorganchem.2022.122596
Publikováno v:
Journal of Asian natural products research. 22(4)
Twelve dihydrostilbenes (including five new analogues) were prepared by the Witting-Hornor reaction from appropriate aromatic aldehydes and phosphonate esters, followed by hydrogenation in five steps. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b5d879fec92b7061cdf01f01466c2ac
https://pubmed.ncbi.nlm.nih.gov/30835549
https://pubmed.ncbi.nlm.nih.gov/30835549
Publikováno v:
Synthetic Communications. 38:973-982
Fifteen 2‐(5‐substituted‐1,3,4‐thiadiazolo‐2‐ylimino)‐4‐thiazolidinones were efficiently synthesized from the reaction of ammonium thiocyanate with 2‐chloro‐N‐(5‐substutited‐1,3,4‐thiadiazolo‐2‐yl)acetamides under micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ec4bd35da1d46caf22b3eea20d6fa20
https://doi.org/10.1080/00397910701845852
https://doi.org/10.1080/00397910701845852
Publikováno v:
ChemInform. 39
Fifteen 2‐(5‐substituted‐1,3,4‐thiadiazolo‐2‐ylimino)‐4‐thiazolidinones were efficiently synthesized from the reaction of ammonium thiocyanate with 2‐chloro‐N‐(5‐substutited‐1,3,4‐thiadiazolo‐2‐yl)acetamides under micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c85c8dc2e327191dcd143e672605b9f
https://doi.org/10.1002/chin.200832134
https://doi.org/10.1002/chin.200832134
Publikováno v:
HETEROCYCLES. 71:2363
An efficient and convenient procedure is described for the preparation of N3-functionalized aminoimidazolines and aminopyrimidines through the aza-Michael additions of aminoimidazolines and aminopyrimidines with a, /?-unsaturated carbonyl compounds c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a512c9f51e296c7342ad98d8912ef2c3
https://doi.org/10.3987/com-07-11118
https://doi.org/10.3987/com-07-11118