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Mendeleev Communications, 2004, Volume 14, Issue 6, Pages 310–312
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002049
(Mi mendc3923)
 

This article is cited in 1 scientific paper (total in 1 paper)

Resolution and racemization of nonbenzenoid atropenantiomers

P. V. Novikova, O. R. Malyshevb, K. A. Lyssenkoc, R. G. Kostyanovskya

a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (198 kB) Citations (1)
Abstract: The three-step synthesis of adduct 3 has been reinvestigated; enantiomers 3a and 3b have been separated by enantioselective chromatography and the racemization barrier of 3a was determined as ΔG = 24.4 kcal mol−1 (16 °C).
Document Type: Article
Language: English


Citation: P. V. Novikov, O. R. Malyshev, K. A. Lyssenko, R. G. Kostyanovsky, “Resolution and racemization of nonbenzenoid atropenantiomers”, Mendeleev Commun., 14:6 (2004), 310–312
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  • This publication is cited in the following 1 articles:
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