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Synthesis of (R)- and (S)-isomers of 2-methylspermidine

Maxim Alekseevich Khomutov 1
Maxim Alekseevich Khomutov
, 
Alexander Olegovich Chizhov 2
Alexander Olegovich Chizhov
, 
Sergei Nikolaevich Kochetkov 1
Sergei Nikolaevich Kochetkov
, 
Alexey Radievich Khomutov 1
Alexey Radievich Khomutov
10.1016/j.mencom.2019.11.025
Published 2019-11-01
Communication , Volume 29, Issue 6, 678-679
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Khomutov M. A. et al. Synthesis of (R)- and (S)-isomers of 2-methylspermidine // Mendeleev Communications. 2019. Vol. 29. No. 6. pp. 678-679.
GOST all authors (up to 50) Copy
Khomutov M. A., Chizhov A. O., Kochetkov S. N., Khomutov A. R. Synthesis of (R)- and (S)-isomers of 2-methylspermidine // Mendeleev Communications. 2019. Vol. 29. No. 6. pp. 678-679.
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TY - JOUR
DO - 10.1016/j.mencom.2019.11.025
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.11.025
TI - Synthesis of (R)- and (S)-isomers of 2-methylspermidine
T2 - Mendeleev Communications
AU - Khomutov, Maxim Alekseevich
AU - Chizhov, Alexander Olegovich
AU - Kochetkov, Sergei Nikolaevich
AU - Khomutov, Alexey Radievich
PY - 2019
DA - 2019/11/01
PB - Mendeleev Communications
SP - 678-679
IS - 6
VL - 29
ER -
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@article{2019_Khomutov,
author = {Maxim Alekseevich Khomutov and Alexander Olegovich Chizhov and Sergei Nikolaevich Kochetkov and Alexey Radievich Khomutov},
title = {Synthesis of (R)- and (S)-isomers of 2-methylspermidine},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.11.025},
number = {6},
pages = {678--679},
doi = {10.1016/j.mencom.2019.11.025}
}
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Khomutov, Maxim Alekseevich, et al. “Synthesis of (R)- and (S)-isomers of 2-methylspermidine.” Mendeleev Communications, vol. 29, no. 6, Nov. 2019, pp. 678-679. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.11.025.

Abstract

The title compounds, (R)- and (S)-isomers of 1,8-diamino-2-methyl-4-azaoctane, were prepared from commercially available enantiomers of 3-bromo-2-methylpropan-1-ol, each in six steps and good overall yields.

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