Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob05816a
Title: Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids
Authors: Jeong, Y.-C.
Anwar, M.
Nguyen, T.M.
Tan, B.S.W.
Chai, C.L.L. 
Moloney, M.G.
Issue Date: 7-Oct-2011
Source: Jeong, Y.-C., Anwar, M., Nguyen, T.M., Tan, B.S.W., Chai, C.L.L., Moloney, M.G. (2011-10-07). Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids. Organic and Biomolecular Chemistry 9 (19) : 6663-6669. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob05816a
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. © 2011 The Royal Society of Chemistry.
Source Title: Organic and Biomolecular Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/105776
ISSN: 14770520
DOI: 10.1039/c1ob05816a
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