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(Alk-1-ynyl)oxiranes in the Reaction of (Alk-1-ynyl)chlorocarbenes with Alkali Metal Alkoxides

Konstantin Nikolaevich Shavrin 1
Konstantin Nikolaevich Shavrin
, 
Valentin Dmitrievich Gvozdev 1
Valentin Dmitrievich Gvozdev
, 
Oleg Matveevich Nefedov 1
Oleg Matveevich Nefedov
10.1070/MC1995v005n05ABEH000513
Published 1995-10-30
Communication , Volume 5, Issue 5, 181-182
6
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Shavrin K. N., Gvozdev V. D., Nefedov O. M. (Alk-1-ynyl)oxiranes in the Reaction of (Alk-1-ynyl)chlorocarbenes with Alkali Metal Alkoxides // Mendeleev Communications. 1995. Vol. 5. No. 5. pp. 181-182.
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Shavrin K. N., Gvozdev V. D., Nefedov O. M. (Alk-1-ynyl)oxiranes in the Reaction of (Alk-1-ynyl)chlorocarbenes with Alkali Metal Alkoxides // Mendeleev Communications. 1995. Vol. 5. No. 5. pp. 181-182.
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TY - JOUR
DO - 10.1070/MC1995v005n05ABEH000513
UR - https://mendcomm.colab.ws/publications/10.1070/MC1995v005n05ABEH000513
TI - (Alk-1-ynyl)oxiranes in the Reaction of (Alk-1-ynyl)chlorocarbenes with Alkali Metal Alkoxides
T2 - Mendeleev Communications
AU - Shavrin, Konstantin Nikolaevich
AU - Gvozdev, Valentin Dmitrievich
AU - Nefedov, Oleg Matveevich
PY - 1995
DA - 1995/10/30
PB - Mendeleev Communications
SP - 181-182
IS - 5
VL - 5
ER -
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@article{1995_Shavrin,
author = {Konstantin Nikolaevich Shavrin and Valentin Dmitrievich Gvozdev and Oleg Matveevich Nefedov},
title = {(Alk-1-ynyl)oxiranes in the Reaction of (Alk-1-ynyl)chlorocarbenes with Alkali Metal Alkoxides},
journal = {Mendeleev Communications},
year = {1995},
volume = {5},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1995v005n05ABEH000513},
number = {5},
pages = {181--182},
doi = {10.1070/MC1995v005n05ABEH000513}
}
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Shavrin, Konstantin Nikolaevich, et al. “(Alk-1-ynyl)oxiranes in the Reaction of (Alk-1-ynyl)chlorocarbenes with Alkali Metal Alkoxides.” Mendeleev Communications, vol. 5, no. 5, Oct. 1995, pp. 181-182. https://mendcomm.colab.ws/publications/10.1070/MC1995v005n05ABEH000513.

Abstract

The reaction of (alk-1-ynyl)chlorocarbenes 2a–c, generated from dichlorides 1a–c, with alkali metal alkoxides 3 gives 2-(alk-1-ynyl)oxiranes 5a–f in 30–70% yield.

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