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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2004 Volume 14, Issue 6, Pages 310–312 (Mi mendc3923)

This article is cited 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

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).

Language: English

DOI: 10.1070/MC2004v014n06ABEH002049



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