Palladium-catalyzed regioselective azidation of allylic C–H bonds under atmospheric pressure of dioxygen
H Chen, W Yang, W Wu, H Jiang
Index: Organic and Biomolecular Chemistry, , vol. 12, # 21 p. 3340 - 3343
Full Text: HTML
Citation Number: 17
Abstract
... Jiao have independently developed novel and elegant methods for the synthesis of organic azides while ... 3-triazoles, 14 thus allowing for the direct ligation of alkenes to biomolecular frameworks via a triazole linker, an approach that could be used in bioconjugate chemistry. ...
Related Articles:
An internally activated tin hydride with enhanced reducing ability
[Vedejs, E.; Duncan, S. M.; Haight, A. R. Journal of Organic Chemistry, 1993 , vol. 58, # 11 p. 3046 - 3050]
[. beta.-(Trimethylsilyl) ethyl] lithium: a new reagent for carbonyl reductive vinylation
[Wilson, Stephen R.; Shedrinsky, Alexander Journal of Organic Chemistry, 1982 , vol. 47, # 10 p. 1983 - 1984]
On the Route to the Photogeneration of Heteroaryl Cations. The Case of Halothiophenes
[Protti, Stefano; Fagnoni, Maurizio; Albini, Angelo Organic and Biomolecular Chemistry, 2005 , vol. 3, # 15 p. 2868 - 2871]
Rhodium-and iridium-catalyzed allylation of electron-rich arenes with allyl tosylate
[Tsukada, Naofumi; Yagura, Yasushige; Sato, Tetsuo; Inoue, Yoshio Synlett, 2003 , # 10 p. 1431 - 1434]
[. beta.-(Trimethylsilyl) ethyl] lithium: a new reagent for carbonyl reductive vinylation
[Journal of Organic Chemistry, , vol. 47, # 10 p. 1983 - 1984]