Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Peiqiu, Liao"'
Publikováno v:
Organic Letters. 24:8136-8141
Publikováno v:
Chemical Communications. 58:13783-13786
An efficient and practical method for the synthesis of benzyl azides from carbonyl compounds and commercially available TMSN3 was developed. The synthetic advantages are illustrated by gram-scale reaction and the synthesis of drug-like molecules.
Autor:
Yong Yang, Shaopeng Liu, Shuang Li, Zhaohong Liu, Peiqiu Liao, Paramasivam Sivaguru, Ying Lu, Jiaojiao Gao, Xihe Bi
Publikováno v:
Angewandte Chemie International Edition. 62
Autor:
Yong, Yang, Shaopeng, Liu, Shuang, Li, Zhaohong, Liu, Peiqiu, Liao, Paramasivam, Sivaguru, Ying, Lu, Jiaojiao, Gao, Xihe, Bi
Publikováno v:
Angewandte Chemie (International ed. in English).
The construction of allylic quaternary sp
Publikováno v:
Synthesis. 52:2111-2120
An efficient and highly regioselective synthesis of isomeric 3-[1-substituted pyrazol-3(5)-yl]indoles has been developed by the acid-mediated regioselective cyclocondensation reaction of β-ethyltho-β-indolyl-α,β-unsaturated ketones and monosubsti
Publikováno v:
European Journal of Organic Chemistry. 2020:693-696
Publikováno v:
Chemical Research in Chinese Universities. 36:847-852
A green and efficient synthesis of 3-pyrazolyl indoles was developed by the cyclocondensation reaction of β-ethylthio-β-indolyl-α, β-unsaturated ketones with semicarbazide hydrochloride as hydrazine equivalent in the presence of 3 equiv. of PEG-4
Publikováno v:
Synlett. 28:1828-1834
A novel FeCl3·6H2O-catalyzed tandem Friedel–Crafts alkylation–hydrolysis reaction between chain α-oxo ketene dithioacetals and alcohols to afford α-alkylated β-oxo thioesters has been successfully developed. The reaction is efficient in the p
Publikováno v:
European Journal of Organic Chemistry. 2017:1289-1293
A green and efficient cyclocondensation reaction of β-ethylthio-β-indolyl-α, β-unsaturated ketones with semicarbazide hydrochloride as hydrazine equivalent to prepare 3-pyrazolyl indoles had been developed in the presence of 3 equiv. of PEG-400 i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84efdf952f7211f9566732f330f683b3
https://doi.org/10.3762/bxiv.2019.118.v1
https://doi.org/10.3762/bxiv.2019.118.v1