Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Zhengneng Jin"'
Publikováno v:
Organic Letters. 25:2691-2695
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d962f5c980a2ee6793d2ca5427829bdf
https://doi.org/10.1021/acs.orglett.3c00782
https://doi.org/10.1021/acs.orglett.3c00782
Autor:
Rurong Yu, Feiyue Hao, Xinyu Zhang, Zhongbing Fang, Zhengneng Jin, Guyue Liu, Guoliang Dai, Jiashou Wu
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc25247178805a1e57b4b28a6516914
https://doi.org/10.1021/acs.joc.3c00283
https://doi.org/10.1021/acs.joc.3c00283
Publikováno v:
European Journal of Organic Chemistry. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0248676f0b2da163e6695b5e401a3bc
https://doi.org/10.1002/ejoc.202300071
https://doi.org/10.1002/ejoc.202300071
Publikováno v:
Advanced Synthesis & Catalysis. 364:1889-1895
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a2320324588b81b62fea7436472d4c6
https://doi.org/10.1002/adsc.202200140
https://doi.org/10.1002/adsc.202200140
Publikováno v:
In Dyes and Pigments January 2013 96(1):204-210
Publikováno v:
ChemistrySelect. 5:6626-6629
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::254ba28a754a61b5c95a2c464877e744
https://doi.org/10.1002/slct.202002037
https://doi.org/10.1002/slct.202002037
Publikováno v:
Organic Chemistry Frontiers. 6:3562-3565
We have developed a transition metal free method for efficient and chemoselective reduction of CO bonds using DMF as a hydrogen source and solvent. α-Ketoamides bearing various functional groups are smoothly reduced to α-hydroxyamides in high yield
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f222533be15185163fcdf48634b8389
https://doi.org/10.1039/c9qo00842j
https://doi.org/10.1039/c9qo00842j
Publikováno v:
Synlett. 29:1061-1064
A redox annulation reaction of cyclic amines and α-ketoamides was developed. A variety of 1,2-fused bicyclic imidazolidin-4-ones were synthesized in moderate to good yields from cyclic amines by redox-neutral α-C–H functionalization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b67fb62ad536267831b5c4f8023bce75
https://doi.org/10.1055/s-0036-1591951
https://doi.org/10.1055/s-0036-1591951
Autor:
Zhengneng Jin, Zhong-Bing Fang, Guo-Liang Dai, Wu-Bing Yao, Jiashou Wu, Ru-Rong Yu, Feiyue Hao, Guyue Liu
Publikováno v:
Tetrahedron Letters. 86:153524
An efficient and practical method for chemoselective “on-water” reduction of α-keto amide by Hantzsch ester without using any catalysts and additives was developed. Control experiments indicated that the intramolecular hydrogen bond of α-keto a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de9efc7950d88638fc84915322757b7a
https://doi.org/10.1016/j.tetlet.2021.153524
https://doi.org/10.1016/j.tetlet.2021.153524
Publikováno v:
Tetrahedron Letters. 58:546-551
An efficient and practical method was developed for the synthesis of tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones based on the decarboxylative cyclization reaction of α-ketoamides and proline. In most cases, tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::255e3f249ad8b864675a0287104bb73e
https://doi.org/10.1016/j.tetlet.2016.12.079
https://doi.org/10.1016/j.tetlet.2016.12.079