Pyrrolidine synthons for β-lactams
- Authors: Valiullina Z.R.1, Lobov A.N.1, Selezneva N.K.1, Miftakhov M.S.1
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Affiliations:
- Ufa Institute of Organic Chemistry
- Issue: Vol 52, No 3 (2016)
- Pages: 349-354
- Section: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/213866
- DOI: https://doi.org/10.1134/S1070428016030106
- ID: 213866
Cite item
Abstract
Fused tricyclic aziridines, methyl rel-(2R,2aR,3R,4R,4aR,4bS)- and rel-(2S,2aR,3R,4R,4aR,4bS)-4-hydroxy-2,4a-dimethoxyhexahydro-1-oxa-2b-azacyclopropa[cd]pentalene-3-carboxylates, have been synthesized as possible precursors to β-lactams. The product structure has been determined by two-dimensional NMR techniques in combination with computational methods.
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About the authors
Z. R. Valiullina
Ufa Institute of Organic Chemistry
Author for correspondence.
Email: bioreg@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054
A. N. Lobov
Ufa Institute of Organic Chemistry
Email: bioreg@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054
N. K. Selezneva
Ufa Institute of Organic Chemistry
Email: bioreg@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054
M. S. Miftakhov
Ufa Institute of Organic Chemistry
Email: bioreg@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054
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