Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 13, Issue 19, Pages 5444-5449Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ob00066a
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [20702051]
- Natural Science Foundation of Zhejiang Province [LY13B020017]
- Key Innovation Team of Science and Technology in Zhejiang Province [2010R50018]
Ask authors/readers for more resources
By using click-triazoles as conveniently approachable and removable directing groups, the direct palladium-catalyzed C(sp(3))-H arylation of amino acid derivatives with various aryl iodides bearing different electronic properties has been achieved. Notably, the desired amino acid molecule can be obtained by the cleavage of the tethered click-triazoles after the catalytic reaction, which aims to provide a practical protocol for the accessibility of both natural and synthetic amino acids.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available