Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ji-wei REN"'
Autor:
Jing-jing LIU, Xiao-ping LIU, Ji-wei REN, Hong-yan ZHAO, Xu-feng YUAN, Xiao-fen WANG, Abdelfattah Z M Salem, Zong-jun CUI
Publikováno v:
Journal of Integrative Agriculture, Vol 14, Iss 3, Pp 503-513 (2015)
To improve the nutritional value and the palatability of air-dried rice straw, culture broth of the lactic acid bacteria community SFC-2 was used to examine the effects of two different treatments, fermentation and adsorption. Air-dried and chopped r
Externí odkaz:
https://doaj.org/article/e238662d24a649549704156180260022
Publikováno v:
Organic Letters. 23:7497-7502
An efficient triphenylphosphine oxide-catalyzed amidation and esterification for the rapid synthesis of a series of dipeptides, amides, and esters is described. This reaction is applicable to challenging couplings of hindered carboxylic acids with we
An efficient triphenylphosphine oxide (Ph3PO) catalyzed amidation and esterification reaction for rapid synthesis of a series of dipeptides, amides and esters under mild condition is described. This reaction is applicable to challenging couplings of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd5e8c4d67afa7921633f36c29f2f44
https://doi.org/10.26434/chemrxiv-2021-gvm5c-v2
https://doi.org/10.26434/chemrxiv-2021-gvm5c-v2
Autor:
Hua Yang, Fawei Zhu, Xiaoqing Chen, Ji-Wei Ren, Zhen-Zhen Xie, Lan Zheng, Jun-An Xiao, Hao-Yue Xiang, Zhi-Peng Ye, Zhi-Xiong Deng
Publikováno v:
Organic Letters. 21:2166-2170
A one-pot squaramide-catalyzed enantioselective ring-reorganization domino sequence (Michael addition/intramolecular ring-opening/lactamization) of 3-hydroxyoxindole and methyleneindolinone, which can be readily derived from 3-oxindole, has been esta
Publikováno v:
Chemistry – A European Journal. 25:4673-4677
One-pot ring-opening/ring-closure process of combining methyleneindolinone with 3-aminooxindole has been developed in this work. Novel polycyclic spirooxindoles were efficiently assembled under mild conditions in high yields (up to 95 %) with moderat
Autor:
Jun-An Xiao, Ji-Wei Ren, Han-Wen Wu, Dan Song, Hua Yang, Hao-Yue Xiang, Xiaoqing Chen, Zhi-Peng Ye, Peng-Ju Xia
Publikováno v:
Chemical communications (Cambridge, England). 55(18)
A visible-light-induced difluoroalkylation of N,N'-cyclicazomethine imine was successfully realized through a novel photoredox radical-radical cross-coupling reaction. This developed protocol exhibits high functional group tolerance and affords a var
Publikováno v:
European Journal of Organic Chemistry. 2016:1264-1268
With the aid of the hydrogen-bond relay of (S)-camphorsulfonic acid, the enantioselective exo-Diels–Alder cycloaddition of cyclic enones and 2-vinyl-1H-indoles catalyzed by prolinosulfonamide was developed. The corresponding Diels–Alder cycloaddu
Publikováno v:
The Journal of organic chemistry. 82(12)
Hydrogen-bonding organocatalysts L-pyroglutamic sulphonamides were readily synthesized for the first time by fully exploiting the potentials of L-pyroglutamic acid. The newly designed catalyst was successfully applied in catalyzing asymmetric Diels
Publikováno v:
European Journal of Organic Chemistry. 2014:5700-5704
The enantioselective 1,3-dipolar cycloaddition of 2-cyclohexene-1-one and azomethine ylides generated in situ from isatins and amino esters was developed by employing prolinosulfonamides as the catalyst. Consequently, novel polycyclic spirooxindole s
Publikováno v:
ChemInform. 47
The enantioselective DAR of cyclic enones with 2-vinylindoles is achieved with the aid of hydrogen-bond relay from (S)-camphorsulfonic acid.