Zobrazeno 1 - 10
of 304
pro vyhledávání: '"Jie-Ping Wan"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2348-2353 (2018)
The synthesis of 4-acyl-NH-1,2,3-triazoles has been accomplished with high efficiency through the cycloaddition reactions between N,N-dimethylenaminones and tosyl azide. This method is featured with extraordinary sustainability by employing water as
Externí odkaz:
https://doaj.org/article/3506cac9007943ea94497bf99044b927
Publikováno v:
ACS Omega, Vol 2, Iss 11, Pp 7784-7789 (2017)
Externí odkaz:
https://doaj.org/article/4eb0eb98e41e4416b177bf69eccc9e81
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2017-2022 (2017)
The reactions between o-hydroxylphenyl-functionalized enaminones and sulfonyl hydrazines providing 3-sulfenylated chromones via domino chromone ring construction and C(sp2)–H bond sulfenylation have been achieved under transition-metal-free conditi
Externí odkaz:
https://doaj.org/article/7caa06a222834cf0a03a3445e0fd6a74
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1122-1126 (2016)
The synthesis of β-arylated alkylamides via alkyl C–H bond arylation has been realized by means of direct one-pot reactions of acyl chlorides, aryl iodides and 8-aminoquinoline. Depending on the structure of the starting materials, both single and
Externí odkaz:
https://doaj.org/article/35479b0d539d49ac8645c2285f7b4d89
Autor:
Jie-Ping Wan, Yanfeng Jing
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 2209-2222 (2015)
Copper catalysis has been known as a powerful tool for its ubiquitous application in organic synthesis. One of the fundamental utilities of copper catalysis is in the C–N bond formation by using carbon sources and nitrogen functional groups such as
Externí odkaz:
https://doaj.org/article/7cbe5a850d004c29aa29e39e21e0985f
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 287-292 (2014)
The three-component reactions of aldehydes, electron deficient alkynes and ureas/thioureas have been smoothly performed to yield a class of unprecedented 3,4-dihydropyrimidinones and thiones (DHPMs). The reactions are initiated by the key transformat
Externí odkaz:
https://doaj.org/article/6e5f6f9214f5478e9111ed8e6be4b6ee
Publikováno v:
Journal of Organic Chemistry; 8/2/2024, Vol. 89 Issue 15, p11060-11066, 7p
Publikováno v:
Organic Letters. 25:2139-2144
Publikováno v:
The Journal of Organic Chemistry. 88:4833-4838
Publikováno v:
The Journal of Organic Chemistry. 88:4017-4023