| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274108 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
The synthesis of polyketide segments through the vinylogous Mukaiyama aldol reaction is reported. The use of chiral oxazaborolidines allows using terminal substituted ketene acetals and provides access to extended segments and two new chiral centers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Serkan Simsek, Markus Kalesse,