Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Chun-Huan Jiang"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2892-2896 (2014)
Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolcular [1,5]-hydride shift/isomerization reaction has been realized, using the inherent reducing power of 3-pyrrolines. A series of N-arylpyrrole containing
Externí odkaz:
https://doaj.org/article/40c67d14b56e423cb16ce982a13d8392
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 5, Iss 4, Pp 300-309 (2015)
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B
Chronic constipation is a common gastrointestinal disease severely affecting the patient׳s quality of life. The traditional treatment of constipation is the use of laxatives. Recently, several new drugs including lubiprostone, linaclotide and prucal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8acc32737e6e4dc7d88cb416eee141
Publikováno v:
The Journal of Organic Chemistry. 80:1155-1162
A concise synthesis of spiroindolenines from 2-substituted (Me, Et) indoles and 2-(pyrrolidin-1-yl)benzaldehydes has been developed via a [1,5]-hydride shift/cyclization sequence. This method features a wide substrate scope and an operationally simpl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::654e43518818f4ec44b9997dce66c920
https://doi.org/10.1021/jo5026817
https://doi.org/10.1021/jo5026817
Autor:
Ling-Yi Kong, Chang Xu, Dongyin Chen, Chun-Huan Jiang, Ji Zhang, Jie Deng, Hongbin Sun, Xiaoan Wen
Publikováno v:
Tetrahedron. 70:1975-1983
Proton-exchanged montmorillonite (H-mont) was found to be an eco-friendly and cost-effective catalyst for the generation of O -methylated quinone methides (QM) from the corresponding p or o -methoxybenzyl esters and ethers. Nucleophilic trapping of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de432075c3756c0cfcdcf6792d5babc9
https://doi.org/10.1016/j.tet.2014.01.064
https://doi.org/10.1016/j.tet.2014.01.064
Publikováno v:
ChemInform. 46
Optimized conditions A) can be applied to various indoles and benzaldehydes bearing a pyrrolidine moiety in o-position.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dea2f23df4366ef9a28d5a587c9a4b9f
https://doi.org/10.1002/chin.201523187
https://doi.org/10.1002/chin.201523187
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2892-2896 (2014)
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2892-2896 (2014)
Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolcular [1,5]-hydride shift/isomerization reaction has been realized, using the inherent reducing power of 3-pyrrolines. A series of N-arylpyrrole containing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00229862a9912c97c9fcb66aa8501e2d
https://pubmed.ncbi.nlm.nih.gov/25550755
https://pubmed.ncbi.nlm.nih.gov/25550755
Autor:
Hongbin Sun, Jie Deng, Xiaoan Wen, Ji Zhang, Chun-Huan Jiang, Chang Xu, Dongyin Chen, Ling-Yi Kong
Publikováno v:
ChemInform. 45
The operationally simple protocol allows the Friedel-Crafts-like alkylation of arenes and heteroarenes, as well as the etherification of a variety of alcohols with benzyl acetates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c700fa1d2cf922dbdd78970fa9fed92
https://doi.org/10.1002/chin.201434123
https://doi.org/10.1002/chin.201434123
Publikováno v:
Journal of Organic Chemistry; 1/16/2015, Vol. 80 Issue 2, p1155-1162, 8p