Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/30967
Title: Ruthenium Catalyzed Directing Group-Free C2-Selective Carbenoid Functionalization of Indoles by alpha-Aryldiazoesters
Authors: Chan, WW
Yeung, SH
Zhou, Z
Chan, ASC
Yu, WY 
Issue Date: 2010
Publisher: American Chemical Society
Source: Organic letters, 2010, v. 12, no. 3, p. 604-607 How to cite?
Journal: Organic letters 
Abstract: A directing group-free approach for C2-selective carbenoid functionalization of NH-indoles is presented. Using [RuCl(2)(p-cymene)](2) as catalyst and alpha-aryldiazoesters as carbenoid source, 2-alkylated indoles were obtained in up to 96% isolated yield. Similarly, a regioselective carbenoid functionalization of NH-pyrroles was also achieved.
URI: http://hdl.handle.net/10397/30967
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/ol9028226
Appears in Collections:Journal/Magazine Article

Access
View full-text via PolyU eLinks SFX Query
Show full item record

SCOPUSTM   
Citations

59
Citations as of Jul 7, 2017

WEB OF SCIENCETM
Citations

55
Last Week
0
Last month
Citations as of Aug 20, 2017

Page view(s)

42
Last Week
4
Last month
Checked on Aug 20, 2017

Google ScholarTM

Check

Altmetric



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.