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Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones

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Ghochikyan T. V. et al. Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 562-564.
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Ghochikyan T. V., Samvelyan M. A., Galstyan A. S., Muzalevskiy V. M., Nenajdenko V. G. Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 562-564.
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TY - JOUR
DO - 10.1016/j.mencom.2017.11.007
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.007
TI - Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones
T2 - Mendeleev Communications
AU - Ghochikyan, Tariel V
AU - Samvelyan, Melanya A
AU - Galstyan, Armen S
AU - Muzalevskiy, Vasilii Mikhailovich
AU - Nenajdenko, Valentin Georgievich
PY - 2017
DA - 2017/10/30
PB - Mendeleev Communications
SP - 562-564
IS - 6
VL - 27
ER -
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@article{2017_Ghochikyan,
author = {Tariel V Ghochikyan and Melanya A Samvelyan and Armen S Galstyan and Vasilii Mikhailovich Muzalevskiy and Valentin Georgievich Nenajdenko},
title = {Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.007},
number = {6},
pages = {562--564},
doi = {10.1016/j.mencom.2017.11.007}
}
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Ghochikyan, Tariel V., et al. “Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones.” Mendeleev Communications, vol. 27, no. 6, Oct. 2017, pp. 562-564. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.007.

Abstract

Copper catalyzed [2 + 3] cycloaddition of 3-propargyl- γ-butyrolactones with azides affords the corresponding 1,2,3-triazoles connected with lactone moiety in high yields. In the presence of air and copper(i) halides, the starting propargylated lactones are prone to dimerize to form bis-lactone diynes.

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