Journal
ORGANIC LETTERS
Volume 20, Issue 2, Pages 333-336Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b03544
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Funding
- National Natural Science Foundation of China [21472028]
- National Key Technologies RD Program [2014BAD23B01]
- Thousand Talent Plan
- 10 Talent Plan (Shicengci) of Guizhou Province
- Guizhou Province Returned Oversea Student Science and Technology Activity Program
- Guizhou University (China)
- Singapore National Research Foundation [NRF-NRFI2016-06]
- Ministry of Education of Singapore [MOE2013-T2-2-003, MOE2016-T2-1-032, RG108/16]
- A*STAR Individual Research Grant [A1783c0008]
- Nanyang Technological University
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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 sp(3)-carbons of aryl carboxylic esters.
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