Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Liu-Lan Shen"'
Publikováno v:
Organic & Biomolecular Chemistry. 14:623-630
In this study, we executed an effective and novel enantioselective Michael/cyclodehydration sequential reaction between pyrazolin-5-one (or 4-hydroxy-2-pyrone) and chalcones that is catalyzed by a quinine-derived primary amine L7 in the presence of B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55855b8522190e9609412011c332ecca
https://doi.org/10.1039/c5ob01656h
https://doi.org/10.1039/c5ob01656h
Publikováno v:
Synlett. 26:970-974
A simple and highly atom-economical method for the direct N-alkylation of aromatic amines by using a microflow reactor was developed to overcome the problem of over-alkylation. In the developed method, high-yield conversion (up to 100%) was achieved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45ac7415864a7521ae11a16d66796cf3
https://doi.org/10.1055/s-0034-1379895
https://doi.org/10.1055/s-0034-1379895
Publikováno v:
ChemInform. 47
In this study, we executed an effective and novel enantioselective Michael/cyclodehydration sequential reaction between pyrazolin-5-one (or 4-hydroxy-2-pyrone) and chalcones that is catalyzed by a quinine-derived primary amine L7 in the presence of B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebfe1bb49f56e42e7c4d237623096a50
https://doi.org/10.1002/chin.201620140
https://doi.org/10.1002/chin.201620140
Autor:
Shuo-Bin Chen, Jie-Bin Ou, Jia-Heng Tan, Ding Li, Zhi-Shu Huang, Tian-Miao Ou, Liu-Lan Shen, Lian-Quan Gu, Shi-Liang Huang, Zhi-Hong Huang, Wei-Bin Wu
Publikováno v:
European Journal of Medicinal Chemistry. 46:3339-3347
A series of mansonone F (MF) derivatives were designed and synthesized. These compounds were found to be strong inhibitors for topoisomerases, with much more significant inhibition for topoisomerase II rather than topoisomerase I. The best inhibitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30e0064cc5de0c3fa3a86ba802559d9d
https://doi.org/10.1016/j.ejmech.2011.04.059
https://doi.org/10.1016/j.ejmech.2011.04.059
Publikováno v:
Journal of Carbohydrate Chemistry. 30:119-131
This report describes the efficient synthesis of quercetin 3-O-[6″-O-(trans-p-coumaroyl)]-β-D-glucopyranoside 1 (isoquercitrin coumarate), an acylated quercetin glycoside possessing antihypertensive, antidiabetic, and tyrosinase inhibitory activit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c780bed997b37c3f28a1f7739d7ebf3
https://doi.org/10.1080/07328303.2011.616979
https://doi.org/10.1080/07328303.2011.616979
Publikováno v:
European Journal of Organic Chemistry. 2010:6895-6899
Dimethylaluminium methaneselenolate (Me 2 AlSeMe, 1) acts as an acyl transfer agent for esterification. In cases of direct macrolactonisation (n = 10-12), this selenium-aluminium complex preferentially creates symmetric macrodiolides rather than macr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6680628eebc77fe1fc2cc1aa878c964
https://doi.org/10.1002/ejoc.201001201
https://doi.org/10.1002/ejoc.201001201
Publikováno v:
Tetrahedron: Asymmetry. 19:1647-1653
The solvent-dependent enzyme reactivity of porcine pancreatic lipase (PPL)-catalyzed hydrolysis was investigated using trans - 3 and cis -(3-(benzyloxymethyl)oxiran-2-yl)methyl acetate 4 as substrates. The conversion efficiency and enantioselectivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f3114833caf8b1f3c838831dfd2fa21
https://doi.org/10.1016/j.tetasy.2008.05.021
https://doi.org/10.1016/j.tetasy.2008.05.021
Publikováno v:
Archives of Pharmacal Research. 27:816-819
Many diselenide compounds are used as antioxidants, enzyme inhibitors and cytokine inducers. Three new diselenide compounds, bis-(2-hydroxyphenyl) diselenide, bis-(3-hydroxyphenyl) diselenide and bis-(4-hydroxyphenyl) diselenide were designed and syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::696580a63a2f65db574d5007b700c316
https://doi.org/10.1007/bf02980171
https://doi.org/10.1007/bf02980171
Publikováno v:
Chemistry Letters. 40:1135-1137
Resokaempferol 3-O-β-D-glucoside, an artificial flavonol glycoside, was synthesized from 2,4-dihydroxyacetophenone in six steps and 40% overall yield via an efficient glycosylation method using NaH.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95080942f355cd7b3076a0ed3f86a7fb
https://doi.org/10.1246/cl.2011.1135
https://doi.org/10.1246/cl.2011.1135
Publikováno v:
ChemInform. 43
The synthesis of title compound (VI) from the inexpensive starting material (I) is achieved via an efficient glycosylation for the reaction of compound (III) with the glucopyranosyl bromide (IV).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e45d9d32834037e6582d999581df5517
https://doi.org/10.1002/chin.201212204
https://doi.org/10.1002/chin.201212204