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Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers

Igor Viktorovich Vystorop 1
Igor Viktorovich Vystorop
Gennady Vital'evich Shustov 2
Gennady Vital'evich Shustov
Arvi Rauk 3
Arvi Rauk
Remir Grigorevich Kostyanovsky 2
Remir Grigorevich Kostyanovsky
Published 1994-06-30
CommunicationVolume 4, Issue 3, 97-99
4
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Vystorop I. V. et al. Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers // Mendeleev Communications. 1994. Vol. 4. No. 3. pp. 97-99.
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Vystorop I. V., Shustov G. V., Rauk A., Kostyanovsky R. G. Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers // Mendeleev Communications. 1994. Vol. 4. No. 3. pp. 97-99.
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TY - JOUR
DO - 10.1070/MC1994v004n03ABEH000366
UR - https://mendcomm.colab.ws/publications/10.1070/MC1994v004n03ABEH000366
TI - Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers
T2 - Mendeleev Communications
AU - Vystorop, Igor Viktorovich
AU - Shustov, Gennady Vital'evich
AU - Rauk, Arvi
AU - Kostyanovsky, Remir Grigorevich
PY - 1994
DA - 1994/06/30
PB - Mendeleev Communications
SP - 97-99
IS - 3
VL - 4
ER -
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@article{1994_Vystorop,
author = {Igor Viktorovich Vystorop and Gennady Vital'evich Shustov and Arvi Rauk and Remir Grigorevich Kostyanovsky},
title = {Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers},
journal = {Mendeleev Communications},
year = {1994},
volume = {4},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1994v004n03ABEH000366},
number = {3},
pages = {97--99},
doi = {10.1070/MC1994v004n03ABEH000366}
}
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Vystorop, Igor Viktorovich, et al. “Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers.” Mendeleev Communications, vol. 4, no. 3, Jun. 1994, pp. 97-99. https://mendcomm.colab.ws/publications/10.1070/MC1994v004n03ABEH000366.

Abstract

The correlation of the Cotton effect sign of the n → π* transition with the cage structure chirality and the absolute configuration of 1,4-dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-diones has been established.

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