Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Hong-Ying Niu"'
Publikováno v:
ARKIVOC, Vol 2010, Iss 9, Pp 300-307 (2010)
Externí odkaz:
https://doaj.org/article/d36f27435d4f40c68fdf01bdc853db74
Autor:
Lei Liang, Yue-Hui Wang, Chen Li, Hua-Jie Wang, Qi-Liang Yang, Chang-Gong Li, Gui-Rong Qu, Hai-Ming Guo, Hong-Ying Niu
Publikováno v:
Organic Chemistry Frontiers. 9:5832-5839
Dehydrogenative coupling of arenes with fluoroaryl nucleophiles enables the efficient synthesis of fluoroaromatic compounds from readily available starting materials.
Publikováno v:
Organic Letters. 23:8575-8579
We describe Cu-catalyzed intermolecular alkynylation and allylation of unactivated C(sp3)-H bonds with singly occupied molecular orbital-philes (SOMO-philes) via hydrogen atom transfer (HAT). Employing N-fluoro-sulfonamide as a HAT reagent, a set of
Autor:
Renlong Li, Xiongbo Zhang, Minghao Dong, Cheng-Xing Cui, Wanqing Zhang, Ji-Chao Wang, Kai Zhang, Tao Jia, Hong-Ying Niu, Fei Huang
Publikováno v:
Dyes and Pigments. 209:110908
Autor:
Hai-Ming Guo, Ren-Long Li, Hong-Ying Niu, Jin-Kai Yan, Lei Liang, Chang-Gong Li, Yao-Fei Wang
Publikováno v:
Organic Letters. 22:6842-6846
The classical Sonogashira reaction of aryl electrophiles in the presence of Pd catalysts has been well established as a potent method for arylalkyne synthesis. However, the site-selective C(sp2)–C(...
Publikováno v:
Chemical Communications. 55:553-556
Intermolecular asymmetric dearomative 1,3-dipolar cycloaddition of 2-nitrobenzofurans with azomethine ylides was enabled by using a chiral Cu(i)/(S,Sp)-iPr-Phosferrox catalyst. As a result, a series of highly stereoselective chiral [2,3]-fused hydrob
Autor:
Lei, Liang, Hong-Ying, Niu, Ren-Long, Li, Yao-Fei, Wang, Jin-Kai, Yan, Chang-Gong, Li, Hai-Ming, Guo
Publikováno v:
Organic letters. 22(17)
The classical Sonogashira reaction of aryl electrophiles in the presence of Pd catalysts has been well established as a potent method for arylalkyne synthesis. However, the site-selective C(sp
Publikováno v:
Organic Letters. 20:5398-5401
A direct route to chiral six-membered carbocyclic purine nucleoside analogues with three chiral stereocenters, including a chiral tetrasubstituted carbon center, via a highly enantioselective [3 + 3] annulation has been established. With the applicat
Publikováno v:
Advanced Synthesis & Catalysis. 360:2813-2819
Publikováno v:
Organic Chemistry Frontiers. 5:3148-3152
An atom-economic addition of pyrimidines to allenes has been developed for the diverse synthesis of branched or linear N-allylpyrimidine analogues. With [Rh(COD)Cl]2/chiral MeOBIPHEP as the catalyst, the asymmetric allylation reaction proceeded well