Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jingzhao Xia"'
Autor:
Wanbin Zhang, Haruki Nagae, Takahiro Hirai, Jingzhao Xia, Shoichiro Katayama, Kazushi Mashima
Publikováno v:
ACS Catalysis. 11:6643-6655
Publikováno v:
Annals of Palliative Medicine. 9:3332-3339
BACKGROUND The study aimed to confirm the important role of ozone autologous blood therapy (autohemotherapy) in promoting successful finger replantation and its possible influence mechanism. METHODS A total of 150 patients with severed finger replant
Publikováno v:
Chemistry - An Asian Journal. 13:1897-1901
A PdII -catalyzed oxidative tandem cyclization was developed for the construction of fused 5,6-bicyclic N, O-heterocycles. This reaction was enabled by the combined use of a 3-methylpyridine ligand and pentafluorobenzoic acid additive. A range of het
Publikováno v:
Chinese Journal of Chemistry. 36:612-618
Publikováno v:
Organic Chemistry Frontiers. 4:1601-1605
An efficient asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles using an Ir catalyst with an axially flexible chiral phosphine-oxazoline ligand was developed and chiral 3-substituted pyrrolidines could be prepared with excellent ee. 3-Subs
Publikováno v:
Chemistry - A European Journal. 22:18354-18357
An iridium-catalyzed asymmetric hydrogenation of unfunctionalized exocyclic C=C bonds was performed by using an axially flexible chiral phosphine-oxazoline ligand, providing the desired chiral 1-benzyl-2,3-dihydro-1H-indene products with up to 98 % e
Autor:
Chenghao, Ye, Xuezhen, Kou, Jingzhao, Xia, Guoqiang, Yang, Li, Kong, Quhao, Wei, Wanbin, Zhang
Publikováno v:
Chemistry, an Asian journal.
A Pd
Publikováno v:
Organic letters. 19(18)
A highly efficient (aS)-Ir/In-BiphPHOX-catalyzed asymmetric hydrogenation of substituted 2H-chromenes and substituted benzo[e][1,2]oxathiine 2,2-dioxides is described. A series of 2H-chromenes and benzo[e][1,2]oxathiine 2,2-dioxides were hydrogenated
Publikováno v:
Chinese Journal of Chemistry. 36:566-566
Publikováno v:
Organic Letters; Sep2017, Vol. 19 Issue 18, p4884-4887, 4p