Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/79603
Title: C2-Alkylation of N-pyrimidylindole with vinylsilane via cobalt-catalyzed C–H bond activation
Authors: Ding, Zhenhua
Yoshikai, Naohiko
Issue Date: 2012
Source: Ding, Z.,& Yoshikai, N. (2012). C2-Alkylation of N -pyrimidylindole with vinylsilane via cobalt-catalyzed C–H bond activation . Beilstein Journal of Organic Chemistry, 8, 1536-1542.
Series/Report no.: Beilstein journal of organic chemistry
Abstract: Direct C2-alkylation of an indole bearing a readily removable N-pyrimidyl group with a vinylsilane was achieved by using a cobalt catalyst generated in situ from CoBr2, bathocuproine, and cyclohexylmagnesium bromide. The reaction allows coupling between a series of N-pyrimidylindoles and vinylsilanes at a mild reaction temperature of 60 °C, affording the corresponding alkylated indoles in moderate to good yields.
URI: https://hdl.handle.net/10356/79603
http://hdl.handle.net/10220/12709
ISSN: 1860-5397
DOI: 10.3762/bjoc.8.174
Rights: © 2012 The Authors. This paper was published in Beilstein Journal of Organic Chemistry and is made available as an electronic reprint (preprint) with permission of Beilstein-Institut. The paper can be found at the following official DOI: [http://dx.doi.org/ 10.3762/bjoc.8.174]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

SCOPUSTM   
Citations 20

31
checked on Sep 5, 2020

WEB OF SCIENCETM
Citations 20

32
checked on Oct 24, 2020

Page view(s) 20

505
checked on Oct 26, 2020

Download(s) 20

175
checked on Oct 26, 2020

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.