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1,2-Di-tert-butyldiaziridine

Remir Grigorevich Kostyanovsky 1
Remir Grigorevich Kostyanovsky
Vadim A Korneev 1
Vadim A Korneev
Ivan Ivanovich Chervin 1
Ivan Ivanovich Chervin
Vladimir N Voznesensky 1
Vladimir N Voznesensky
Yurii V Puzanov 1
Yurii V Puzanov
Paul Rademacher 2
Paul Rademacher
Published 1996-06-30
CommunicationVolume 6, Issue 3, 106-107
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Kostyanovsky R. G. et al. 1,2-Di-tert-butyldiaziridine // Mendeleev Communications. 1996. Vol. 6. No. 3. pp. 106-107.
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Kostyanovsky R. G., Korneev V. A., Chervin I. I., Voznesensky V. N., Puzanov Y. V., Rademacher P. 1,2-Di-tert-butyldiaziridine // Mendeleev Communications. 1996. Vol. 6. No. 3. pp. 106-107.
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TY - JOUR
DO - 10.1070/MC1996v006n03ABEH000601
UR - https://mendcomm.colab.ws/publications/10.1070/MC1996v006n03ABEH000601
TI - 1,2-Di-tert-butyldiaziridine
T2 - Mendeleev Communications
AU - Kostyanovsky, Remir Grigorevich
AU - Korneev, Vadim A
AU - Chervin, Ivan Ivanovich
AU - Voznesensky, Vladimir N
AU - Puzanov, Yurii V
AU - Rademacher, Paul
PY - 1996
DA - 1996/06/30
PB - Mendeleev Communications
SP - 106-107
IS - 3
VL - 6
ER -
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@article{1996_Kostyanovsky,
author = {Remir Grigorevich Kostyanovsky and Vadim A Korneev and Ivan Ivanovich Chervin and Vladimir N Voznesensky and Yurii V Puzanov and Paul Rademacher},
title = {1,2-Di-tert-butyldiaziridine},
journal = {Mendeleev Communications},
year = {1996},
volume = {6},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1996v006n03ABEH000601},
number = {3},
pages = {106--107},
doi = {10.1070/MC1996v006n03ABEH000601}
}
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Kostyanovsky, Remir Grigorevich, et al. “1,2-Di-tert-butyldiaziridine.” Mendeleev Communications, vol. 6, no. 3, Jun. 1996, pp. 106-107. https://mendcomm.colab.ws/publications/10.1070/MC1996v006n03ABEH000601.

Abstract

1,2-Di-tert-butyldiaziridine 1 has been synthesized for the first time and its 1H and 13C NMR spectra studied in comparison with model diaziridines 810. Its photoelectron and mass spectra have been measured and its structure optimized by semiempirical and ab initio calculations; considerable steric deformation of the CH2 ring fragment and mutual approach of tert-butyl groups is shown.

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