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Alkylation of Chlorin p6 N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene

Viktoriya Sergeevna Lebedeva 1
Viktoriya Sergeevna Lebedeva
, 
Fatima Majmudinovna Karmova 1
Fatima Majmudinovna Karmova
, 
Andrey Fedorovich Mironov 1
Andrey Fedorovich Mironov
10.1016/j.mencom.2015.03.012
Published 2015-03-06
Communication , Volume 25, Issue 2, 117-118
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Lebedeva V. S., Karmova F. M., Mironov A. F. Alkylation of Chlorin p6 N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene // Mendeleev Communications. 2015. Vol. 25. No. 2. pp. 117-118.
GOST all authors (up to 50) Copy
Lebedeva V. S., Karmova F. M., Mironov A. F. Alkylation of Chlorin p6 N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene // Mendeleev Communications. 2015. Vol. 25. No. 2. pp. 117-118.
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TY - JOUR
DO - 10.1016/j.mencom.2015.03.012
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.03.012
TI - Alkylation of Chlorin p6 N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene
T2 - Mendeleev Communications
AU - Lebedeva, Viktoriya Sergeevna
AU - Karmova, Fatima Majmudinovna
AU - Mironov, Andrey Fedorovich
PY - 2015
DA - 2015/03/06
PB - Mendeleev Communications
SP - 117-118
IS - 2
VL - 25
ER -
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@article{2015_Lebedeva,
author = {Viktoriya Sergeevna Lebedeva and Fatima Majmudinovna Karmova and Andrey Fedorovich Mironov},
title = {Alkylation of Chlorin p6 N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.03.012},
number = {2},
pages = {117--118},
doi = {10.1016/j.mencom.2015.03.012}
}
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Lebedeva, Viktoriya Sergeevna, et al. “Alkylation of Chlorin p6 N-hydroxycycloimide with the use of 1,8-diazabicyclo[5.4.0]undec-7-ene.” Mendeleev Communications, vol. 25, no. 2, Mar. 2015, pp. 117-118. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.03.012.

Abstract

The hydroxyl group of N-hydroxycycloimide in a chlorin macrocycle is easily alkylated with haloalkanes in the presence of 1,8-diaza- bicyclo[5.4.0]undec-7-ene to give chlorin p6 N-alkoxycycloimides in yields to 80%.

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