Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/104160
Title: | Direct α-functionalization of simple aldehydes via oxidative N-heterocyclic carbene catalysis | Authors: | Mo, Junming Yang, Ruojie Chen, Xingkuan Tiwari, Bhoopendra Chi, Robin Yonggui |
Keywords: | DRNTU::Science::Chemistry::Organic chemistry | Issue Date: | 2012 | Source: | Mo, J., Yang, R., Chen, X., Tiwari, B., & Chi, Y. R. (2013). Direct α-Functionalization of Simple Aldehydes via Oxidative N-Heterocyclic Carbene Catalysis. Organic Letters, 15(1), 50–53. | Series/Report no.: | Organic letters | Abstract: | A direct α-functionalization of simple aldehydes under N-Heterocyclic Carbene (NHC) catalysis and direct generation of ester enolate equivalents from nonfunctionalized aldehydes are disclosed. The catalysis involves selective enolate generation from an oxidatively generated NHC-bounded ester intermediate as a key step. The ester enolate intermediates undergo stereoselective reactions with enones and trifluoromethyl ketones. | URI: | https://hdl.handle.net/10356/104160 http://hdl.handle.net/10220/19446 |
ISSN: | 1523-7060 | DOI: | 10.1021/ol303035r | Schools: | School of Physical and Mathematical Sciences | Rights: | © 2012 American Chemical Society. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SPMS Journal Articles |
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