Asymmetric access to the smallest enolate intermediate via organocatalytic activation of acetic ester
An NHC-catalyzed activation of acetic esters to afford enolate intermediates is disclosed. The catalytically generated triazolium enolate intermediates serve as two-carbon nucleophiles that undergo highly enantioselective reactions with enones and α,β-unsaturated imines to give α-unsubstituted δ-lac...
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Main Authors: | , , , , |
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Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2014
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Subjects: | |
Online Access: | https://hdl.handle.net/10356/104214 http://hdl.handle.net/10220/19450 |
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Institution: | Nanyang Technological University |
Language: | English |
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