Journal
TETRAHEDRON-ASYMMETRY
Volume 24, Issue 20, Pages 1318-1323Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2013.09.002
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Funding
- Russian Foundation for Basic Research [12-03-00724-a]
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The Diels-Alder adducts of the quinolizidine alkaloids N-methylcytisine, (-)-leontidine, and (-)-thermopsine with N-phenylmaleimide have been synthesized. The structures and absolute configurations of the new asymmetric centers of the products were determined by NMR spectroscopy experiments, QC-calculations, and X-ray data. (C) 2013 Elsevier Ltd. All rights reserved.
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