Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids

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
Citation:	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
Appears in Collections:	Staff Publications

There are no files associated with this item.

Check