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A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(–)-lactate

Mikhail Vladimirovich Zlokazov 1
Mikhail Vladimirovich Zlokazov
, 
Vladimir Vsevolodovich Veselovsky 1
Vladimir Vsevolodovich Veselovsky
10.1070/MC1999v009n02ABEH000882
Published 1999-04-01
Communication , Volume 9, Issue 2, 73-74
5
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Zlokazov M. V., Veselovsky V. V. A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(–)-lactate // Mendeleev Communications. 1999. Vol. 9. No. 2. pp. 73-74.
GOST all authors (up to 50) Copy
Zlokazov M. V., Veselovsky V. V. A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(–)-lactate // Mendeleev Communications. 1999. Vol. 9. No. 2. pp. 73-74.
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TY - JOUR
DO - 10.1070/MC1999v009n02ABEH000882
UR - https://mendcomm.colab.ws/publications/10.1070/MC1999v009n02ABEH000882
TI - A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(–)-lactate
T2 - Mendeleev Communications
AU - Zlokazov, Mikhail Vladimirovich
AU - Veselovsky, Vladimir Vsevolodovich
PY - 1999
DA - 1999/04/01
PB - Mendeleev Communications
SP - 73-74
IS - 2
VL - 9
ER -
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@article{1999_Zlokazov,
author = {Mikhail Vladimirovich Zlokazov and Vladimir Vsevolodovich Veselovsky},
title = {A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(–)-lactate},
journal = {Mendeleev Communications},
year = {1999},
volume = {9},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1999v009n02ABEH000882},
number = {2},
pages = {73--74},
doi = {10.1070/MC1999v009n02ABEH000882}
}
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Zlokazov, Mikhail Vladimirovich, and Vladimir Vsevolodovich Veselovsky. “A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(–)-lactate.” Mendeleev Communications, vol. 9, no. 2, Apr. 1999, pp. 73-74. https://mendcomm.colab.ws/publications/10.1070/MC1999v009n02ABEH000882.

Abstract

Based on ethyl (S)-(–)-lactate, an original sequence of highly stereoselective transformations leading to (4S,5E)-4-bromomethylhept-5-enenitrile was developed using rearrangement of a chiral cyclopropyl carbinol as the key step.

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