Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids

Stoncius A, Nahrwold M, Sewald N (2005)
SYNTHESIS 2005(11): 1829-1837.

Journal Article | Published | English

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Abstract
Five suitably protected enantiomerically pure beta(2)-amino acids, homologues of proteinogenic alpha-amino acids, were synthesized from the common chiral precursor, tert-butyl succinyloxazolidinone.
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Stoncius A, Nahrwold M, Sewald N. Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids. SYNTHESIS. 2005;2005(11):1829-1837.
Stoncius, A., Nahrwold, M., & Sewald, N. (2005). Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids. SYNTHESIS, 2005(11), 1829-1837.
Stoncius, A., Nahrwold, M., and Sewald, N. (2005). Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids. SYNTHESIS 2005, 1829-1837.
Stoncius, A., Nahrwold, M., & Sewald, N., 2005. Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids. SYNTHESIS, 2005(11), p 1829-1837.
A. Stoncius, M. Nahrwold, and N. Sewald, “Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids”, SYNTHESIS, vol. 2005, 2005, pp. 1829-1837.
Stoncius, A., Nahrwold, M., Sewald, N.: Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids. SYNTHESIS. 2005, 1829-1837 (2005).
Stoncius, A, Nahrwold, M, and Sewald, Norbert. “Chiral succinate: A precursor for enantiomerically pure beta(2)-amino acids”. SYNTHESIS 2005.11 (2005): 1829-1837.
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