Zobrazeno 1 - 10
of 84
pro vyhledávání: '"John C.‐G. Zhao"'
Publikováno v:
Advanced Synthesis & Catalysis. 365:1585-1590
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71921275eda2310809b7ec0779962ff9
https://doi.org/10.1002/adsc.202300043
https://doi.org/10.1002/adsc.202300043
Publikováno v:
Organic & Biomolecular Chemistry. 21:761-767
β-Enaminyl radicals were synthesized via organocatalysis and used to release alkyl radicals from phenyliodine(iii) dicarboxylates. The latter was used for the direct one-pot alkylation–aminoxidation of styrene derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdbca8f3ecf991b26fbfa75a51277a8f
https://doi.org/10.1039/d2ob01826h
https://doi.org/10.1039/d2ob01826h
Publikováno v:
Chemical Communications. 58:11308-11311
The α-acyloxylketone motif can be found in many important pharmaceuticals and biologically active natural products and their derivatives. Now we have realized a direct synthesis of α-acyloxylketones from ketones and readily available carboxylic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0c9b6f4d65cafa2698886594e56be22
https://doi.org/10.1039/d2cc04016f
https://doi.org/10.1039/d2cc04016f
Publikováno v:
ChemistrySelect. 6:13577-13581
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37801461e915570eb56d0a1f3b9f19ce
https://doi.org/10.1002/slct.202104138
https://doi.org/10.1002/slct.202104138
Publikováno v:
Chemical communications (Cambridge, England). 58(80)
The α-acyloxylcarbonyl motif can be found in many important pharmaceuticals and biologically active natural products and their derivatives. In this manuscript, the direct synthesis of α-acyloxylketones from ketones and readily available carboxylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d53483642aaf7392e84a06bfab68282e
https://pubmed.ncbi.nlm.nih.gov/36125049
https://pubmed.ncbi.nlm.nih.gov/36125049
Publikováno v:
ChemistrySelect. 6:2252-2280
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebd7f2ae8c3c1062480e5e32bf43f10c
https://doi.org/10.1002/slct.202004196
https://doi.org/10.1002/slct.202004196
Publikováno v:
Advanced Synthesis & Catalysis. 362:2419-2426
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efca1314e966b221f94d6ca35eb3a140
https://doi.org/10.1002/adsc.202000227
https://doi.org/10.1002/adsc.202000227
Publikováno v:
Organicbiomolecular chemistry. 20(1)
Both the enamine and iminium catalysis of the MDOs are switchable. Upon switching on both catalytic modes, the MDOs were used for catalyzing the domino Michael/Michael reaction between (E)-7-aryl-7-oxohept-5-enals and trans-cinnamaldehydes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d496abf7874251bec4995776d74507
https://pubmed.ncbi.nlm.nih.gov/34877959
https://pubmed.ncbi.nlm.nih.gov/34877959
Publikováno v:
Current Organocatalysis. 6:171-176
Background: While proline can catalyze the asymmetric direct aldol reactions, its catalytic activity and catalyst turnover are both low. To improve the catalytic efficiency, many prolinebased organocatalysts have been developed. In this regard, proli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a28bd8b52650e5ed2f76498244e70403
https://doi.org/10.2174/2213337206666190301155247
https://doi.org/10.2174/2213337206666190301155247