Ley, SV;
Sheppard, TD;
Myers, RM;
Chorghade, MS;
(2007)
Chiral glycolate equivalents for the asymmetric synthesis of α-hydroxycarbonyl compounds.
Bulletin of the Chemical Society of Japan
, 80
(8)
pp. 1451-1472.
10.1246/bcsj.80.1451.
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Abstract
Chiral glycolic acid equivalents are used extensively for the enantioselective synthesis of α-hydroxycarbonyl compounds. Their efficacy in enolate reactions and their utility in synthetic applications are discussed, highlighting the relevance of these methods to natural product synthesis.
| Type: | Article |
|---|---|
| Title: | Chiral glycolate equivalents for the asymmetric synthesis of α-hydroxycarbonyl compounds |
| DOI: | 10.1246/bcsj.80.1451 |
| Publisher version: | http://dx.doi.org/10.1246/bcsj.80.1451 |
| Language: | English |
| Keywords: | © 2007 The Chemical Society of Japan |
| UCL classification: | UCL UCL > Provost and Vice Provost Offices UCL > Provost and Vice Provost Offices > UCL BEAMS UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry |
| URI: | https://discovery.ucl.ac.uk/id/eprint/170124 |
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