Journal
ORGANIC LETTERS
Volume 4, Issue 17, Pages 2885-2888Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0262688
Keywords
-
Categories
Funding
- NCI NIH HHS [T32CA09112] Funding Source: Medline
- NIGMS NIH HHS [GM58160] Funding Source: Medline
Ask authors/readers for more resources
[GRAPHIC] The use of Pd(2)dba(3) with bulky, electron-rich ligands 1 or 2 and LIN(TMS)(2) as the base for the coupling of amines with aryl halides containing hydroxyl, amide, or enolizable keto groups is described. This protocol expands the utility of palladium-catalyzed C-N bond formation by allowing for the use of aryl halides containing these functional groups, obviating the need for protecting group manipulations.
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