RUS  ENG
Full version
JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1999 Volume 9, Issue 6, Pages 229–231 (Mi mendc4610)

This article is cited in 2 papers

1,4-Dimethyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione: optical resolution, absolute configuration and circular dichroism

I. V. Vystoropa, A. N. Utyenysheva, V. M. Anisimovb, R. G. Kostyanovskyb

a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: The title dilactone has been resolved into its enantiomers (+)-(S,S)-1 and (–)-(R,R)-1, whose absolute configurations were found by X-ray diffraction analysis of intermediate lactonic amide 2a; the magnitude of the n–π* Cotton effect increased with an increase in folding or a diminution in twist of the boat conformation of a dilactone ring.

Language: English

DOI: 10.1070/MC1999v009n06ABEH001192



© Steklov Math. Inst. of RAS, 2025