Skip To Main Content
Yin-Xia Wang on Muck Rack

Yin-Xia Wang

As seen in: Color Research & Application, Wiley Online Library
Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work. Claim your profile

Get in touch with Yin-Xia

Contact Yin-Xia, search articles and posts on X, monitor coverage, and track replies from one place.

Learn more about Muck Rack

Actions

Share this page

Is this you?

As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile

Articles

Visible-Light-Induced Acylsilylation of Nitrosoarenes for Synthesis of N-Arylhydroxamic Acid Silicon Esters

|
By Yin-Xia Wang, Chuang Wang, Yong-Gang Wang, Mei-Jia Chang
| dx.doi.org
Open in Who Shared Issue with article?

Enantioselective Nickel‐Catalyzed C(sp3)−H Activation of Formamides

|
By Yin-Xia Wang, Feng-Ping Zhang, Hao Chen, YUE LI
| Wiley Online Library Verified
Abstract Enantioselective Ni-catalyzed C(sp3)−H activation via C−H nickellation remains an elusive challenge. Herein, we used phosphine oxide (H8-BINAPO) ligated Ni-Al bimetallic catalyst to achieve an enantioselective Ni-catalyzed aliphatic C(sp3)−H activation with up to 95 % yield and up 95 % ee for the first time. Abstract Enantioselective Ni-catalyzed C(sp3)−H bond activation remains an elusive challenge.
Open in Who Shared View Duplicates (2) Issue with article?

Enantioselective Twofold C‐H Annulation of Formamides and Alkynes without Built‐in Chelating Groups

|
By Hao Chen, Yin-Xia Wang, Yu-Xin Luan, Mengchun Ye
| Color Research & Application Verified
Communication Mengchun Ye Corresponding Author E-mail address: mcye@nankai.edu.cn nankai university, chemistry, 94 Weijin Rd, Lihua Bldg 310, 300071 Tianjin, CHINA Search for more papers by this author PDF PDF ShareShare Abstract Twofold C‐H annulation of readily available formamides and alkynes without built‐in chelating groups was achieved, providing a series of chiral ferrocenes in 40‐98% yield and 93‐99% ee.
Open in Who Shared Issue with article?
See all 4 articles