Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/138275
Title: Addition of N-heterocyclic carbene catalyst to aryl esters induces remote C-Si bond activation and benzylic carbon functionalization
Authors: Wang, Hongling
Chen, Xingkuan
Li, Yongjia
Wang, Jilan
Wu, Shuquan
Xue, Wei
Yang, Song
Chi, Robin Yonggui
Keywords: Science::Chemistry::Organic chemistry
Issue Date: 2018
Source: Wang, H., Chen, X., Li, Y., Wang, J., Wu, S., Xue, W., . . ., Chi, R. Y. (2017). Addition of N-heterocyclic carbene catalyst to aryl esters induces remote C-Si bond activation and benzylic carbon functionalization. Organic letters, 20(2), 333-336. doi:10.1021/acs.orglett.7b03544
Journal: Organic letters
Abstract: Through the incorporation of a silicon atom to an aryl carboxylic ester substrate, the resulting C-Si bond can be activated via the addition of a carbene catalyst on a remote site. This strategy allows for efficient functionalization of the benzylic sp3-carbons of aryl carboxylic esters.
URI: https://hdl.handle.net/10356/138275
ISSN: 1523-7060
DOI: 10.1021/acs.orglett.7b03544
Schools: School of Physical and Mathematical Sciences 
Rights: © 2017 American Chemical Society. All rights reserved. This paper was published in Organic letters and is made available with permission of American Chemical Society.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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