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DOI: 10.1055/s-0037-1609732
Brønsted Acid Catalyzed Dehydrative Arylation of 4-Indolylmethanols with Indoles: Efficient Access to Indolyl-Substituted Triarylmethanes
We are much appreciated for the financial support from NSFC (21772069 and 21702077), the Natural Science Foundation of Jiangsu Province (BK20160003 and BK20170227), TAPP, and Six Kinds of Talents Project of Jiangsu Province (SWYY-025).Publication History
Received: 13 March 2018
Accepted after revision: 30 March 2018
Publication Date:
29 May 2018 (online)
Abstract
A Brønsted acid catalyzed dehydrative arylation of 4-indolylmethanols with indoles has been established, leading to a series of indolyl-substituted triarylmethanes in good to excellent yields (up to 97% yield). In addition, in this Brønsted acid catalyzed dehydration process, the only byproduct was water. Accordingly, this approach can be considered to have high atom economy and to be environmentally friendly. This approach not only provides a useful strategy for the synthesis of structurally diversified indolyl-substituted triarylmethanes, but also represents the first example of a 4-indolylmethanol-involved reaction, which will advance the chemistry of indolylmethanols.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1609732.
- Supporting Information
- CIF File
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For selected examples, see:
For selected reviews, see:
For selected reviews, see:
For selected examples, see:
For related reviews on indolylmethanols, see:
For related reviews on the generation of carbocation from alcohols:
For selected examples on substitutions of 3-indolylmethanols, see:
For selected examples on [3+2] cyclizations of 3-indolylmethanols, see:
For selected examples on [3+3] cyclizations of 3-indolylmethanols, see:
For selected examples on [4+3] cyclizations of 3-indolylmethanols, see:
For selected examples on substitutions of 2-indolylmethanols, see:
For selected examples on cyclizations of 2-indolylmethanols, see: