TY  - JOUR
ID  - publicatio17869
N2  - The synthesis of N-allylic indoles is of great interest because of their potential biological properties. It is a true challenge to develop new methods for the N-allylation of indoles due to the favorable C3-allylation. We uncovered a new strategy to synthesize N-allylic indoles via a palladium catalyst as a promoting agent, providing the N-allylated indoles in high yields. In addition, the organic reaction with polyethylene glycol (PEG) in water is one of the key emerging strategies that is currently attracting tremendous attention, which is intended to provide alternative eco-friendly and efficient ways for the construction of covalent bonds. In this study, the palladium-catalyzed indoles with allylic acetates in a PEG-water system were investigated under various conditions. This system provides a simple, convenient, and efficient way to afford a high yield of N-allylated indoles.
IS  - 29
AV  - restricted
TI  - Palladium-catalyzed selective N-allylation of indoles assisted by PEG-water system
Y1  - 2019///
JF  - NEW JOURNAL OF CHEMISTRY
N1  - Funding Agency and Grant Number: National Science Council of Republic of ChinaNational Science Council of Taiwan [NSC101-2113-M-037-008-MY3]
            Funding text: This work was supported by a grant from the National Science Council of Republic of China (NSC101-2113-M-037-008-MY3).
UR  - http://doi.org/10.1039/c9nj02335f
A1  -  Peng Bai-Jing
A1  -  Huang Yi-Ting
A1  -  Fülöp Ferenc
A1  -  Lin I-Ling
A1  -  Yang Shyh-Chyun
SN  - 1144-0546
SP  - 11549
EP  - 11553
VL  - 43
ER  -