Abstract
An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to diversely substituted systems from a common starting material.
Original language | English |
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Pages (from-to) | 6663-6669 |
Number of pages | 7 |
Journal | Organic and Biomolecular Chemistry |
Volume | 9 |
Issue number | 19 |
DOIs | |
Publication status | Published - 7 Oct 2011 |
Externally published | Yes |