Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Zhuo‐qun Xin"'
Autor:
René Peters, Daniel F. Fischer, Sascha Jautze, Florian M. Koch, Thomas Kull, Paolo S. Tiseni, Zhuo-Qun Xin, Marian Zajac
Publikováno v:
CHIMIA, Vol 62, Iss 6 (2008)
This account summarizes the activities of the first three years of our young research group working in the field of homogeneous asymmetric catalysis.
Externí odkaz:
https://doaj.org/article/d189395aef5b4853848d4471f62d89b0
Publikováno v:
Chemistry - An Asian Journal. 5:1770-1774
The first kinetic resolution of allylic trifluoroacetimidates is achieved by using planar chiral palladacycles as catalysts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::398f1d81e04895026996eb904aac0a84
https://doi.org/10.1002/asia.201000386
https://doi.org/10.1002/asia.201000386
Publikováno v:
Chemistry - A European Journal. 15:8722-8741
Systematic studies have been performed to develop highly efficient catalysts for the asymmetric aza-Claisen rearrangement of trihaloacetimidates. Herein, we describe the stepwise development of these catalyst systems involving four different catalyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c20d2aca091fbb99ad7149b92f68493f
https://doi.org/10.1002/chem.200900712
https://doi.org/10.1002/chem.200900712
Publikováno v:
Synlett. 2008:1495-1499
A catalytic asymmetric synthesis of unprotected secondary allylic amines based on the aza-Claisen rearrangement of N-aryl- and N-alkyl-substituted trifluoroacetimidates has been developed, which provides the targeted products with excellent enantiose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::773eecef31db1df3715e45d0154bfdf0
https://doi.org/10.1055/s-2008-1077792
https://doi.org/10.1055/s-2008-1077792
Publikováno v:
Angewandte Chemie. 119:7848-7851
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5685601bf42eddabf1ed55081f1480bf
https://doi.org/10.1002/ange.200702086
https://doi.org/10.1002/ange.200702086
Publikováno v:
Angewandte Chemie International Edition. 46:7704-7707
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2116196b135db10ef0f1d320065aeb2
https://doi.org/10.1002/anie.200702086
https://doi.org/10.1002/anie.200702086
Autor:
Zhuo‐qun Xin, René Peters, W. Bernd Schweizer, Daniel F. Fischer, Sascha Jautze, Matthias E. Weiss
Publikováno v:
Angewandte Chemie. 118:5823-5827
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0efddbf1f7fd0a7616808bc48b8a5f5e
https://doi.org/10.1002/ange.200601731
https://doi.org/10.1002/ange.200601731
Publikováno v:
Organometallics. 25:2917-2920
Convenient synthetic routes to enantiomerically pure 1‘,2‘,3‘,4‘,5‘-pentamethyl and -pentaphenylferrocenyl imidazolines are described. While the former complexes were diastereoselectively ortho-lithiated and subsequently functionalized by t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9300c71ce14eb4cdfbf1cb4f824cc7d5
https://doi.org/10.1021/om060187o
https://doi.org/10.1021/om060187o
Publikováno v:
Synthetic Communications. 33:2787-2792
The weak basic bicarbonate-activated hydrogen peroxide is applied to the catalytic asymmetric epoxidation of the enones, and the catalyst polyleucine cannot be deteriorated and can successfully be reused in this asymmetric reaction. The ee value of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::face7b2604590fa885866a525cdbad7a
https://doi.org/10.1081/scc-120022166
https://doi.org/10.1081/scc-120022166
Publikováno v:
Tetrahedron: Asymmetry. 13:1937-1940
Asymmetric oxidative coupling of ( S )-1-(3-hydroxy-2-naphthylcarbonyl)pyrrolidine-2-carboxylic acid methyl ester 1 catalyzed by CuCl afforded ( S , S , R )-2,2′-dihydroxy-3,3′-bis(2-methoxycarbonyl-1-pyrrolidinylcarbonyl)-1,1′-binapthalene 2 w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5571bf12fdf5191c93a46969222e4309
https://doi.org/10.1016/s0957-4166(02)00507-4
https://doi.org/10.1016/s0957-4166(02)00507-4