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Subsequent Peripheral Cyclopropanation as a Synthetic Approach to Cyclic and Cyclo-substituted Triangulanes

Nikolai Serafimovich Zefirov 1
Nikolai Serafimovich Zefirov
, 
Tamara Stepanovna Kuznetsova 1
Tamara Stepanovna Kuznetsova
, 
Olga Vladimirovna Eremenko 1
Olga Vladimirovna Eremenko
, 
Olga Vladimirovna Kokoreva 1
Olga Vladimirovna Kokoreva
10.1070/MC1993v003n03ABEH000237
Published 1993-06-30
Communication , Volume 3, Issue 3, 91-92
6
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Zefirov N. S. et al. Subsequent Peripheral Cyclopropanation as a Synthetic Approach to Cyclic and Cyclo-substituted Triangulanes // Mendeleev Communications. 1993. Vol. 3. No. 3. pp. 91-92.
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Zefirov N. S., Kuznetsova T. S., Eremenko O. V., Kokoreva O. V. Subsequent Peripheral Cyclopropanation as a Synthetic Approach to Cyclic and Cyclo-substituted Triangulanes // Mendeleev Communications. 1993. Vol. 3. No. 3. pp. 91-92.
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TY - JOUR
DO - 10.1070/MC1993v003n03ABEH000237
UR - https://mendcomm.colab.ws/publications/10.1070/MC1993v003n03ABEH000237
TI - Subsequent Peripheral Cyclopropanation as a Synthetic Approach to Cyclic and Cyclo-substituted Triangulanes
T2 - Mendeleev Communications
AU - Zefirov, Nikolai Serafimovich
AU - Kuznetsova, Tamara Stepanovna
AU - Eremenko, Olga Vladimirovna
AU - Kokoreva, Olga Vladimirovna
PY - 1993
DA - 1993/06/30
PB - Mendeleev Communications
SP - 91-92
IS - 3
VL - 3
ER -
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@article{1993_Zefirov,
author = {Nikolai Serafimovich Zefirov and Tamara Stepanovna Kuznetsova and Olga Vladimirovna Eremenko and Olga Vladimirovna Kokoreva},
title = {Subsequent Peripheral Cyclopropanation as a Synthetic Approach to Cyclic and Cyclo-substituted Triangulanes},
journal = {Mendeleev Communications},
year = {1993},
volume = {3},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1993v003n03ABEH000237},
number = {3},
pages = {91--92},
doi = {10.1070/MC1993v003n03ABEH000237}
}
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Zefirov, Nikolai Serafimovich, et al. “Subsequent Peripheral Cyclopropanation as a Synthetic Approach to Cyclic and Cyclo-substituted Triangulanes.” Mendeleev Communications, vol. 3, no. 3, Jun. 1993, pp. 91-92. https://mendcomm.colab.ws/publications/10.1070/MC1993v003n03ABEH000237.

Abstract

A general scheme for cyclo-substituted triangulane synthesis has been developed, based on subsequent cyclopropanation of olefinic structures of type 5 and 6.

References

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Triangulanes: stereoisomerism and general method of synthesis
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Journal of the American Chemical Society, 1990
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Journal of Organic Chemistry, 1992
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