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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. Novikov
a
,
O. R. Malyshev
b
,
K. A. Lyssenko
c
,
R. G. Kostyanovsky
a
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 Δ
G
≠
= 24.4 kcal mol
−1
(16 °C).
Language:
English
DOI:
10.1070/MC2004v014n06ABEH002049
Fulltext:
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