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Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling

Elena Sergeevna Matyugina 1
Elena Sergeevna Matyugina
, 
Anastasia Lvovna Khandazhinskaya 1
Anastasia Lvovna Khandazhinskaya
, 
Sergei Nikolaevich Kochetkov 1
Sergei Nikolaevich Kochetkov
, 
Katherine L Seley-Radtke 2
Katherine L Seley-Radtke
10.1016/j.mencom.2020.03.034
Published 2020-03-02
Communication , Volume 30, Issue 2, 231-232
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Matyugina E. S. et al. Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling // Mendeleev Communications. 2020. Vol. 30. No. 2. pp. 231-232.
GOST all authors (up to 50) Copy
Matyugina E. S., Khandazhinskaya A. L., Kochetkov S. N., Seley-Radtke K. L. Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling // Mendeleev Communications. 2020. Vol. 30. No. 2. pp. 231-232.
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TY - JOUR
DO - 10.1016/j.mencom.2020.03.034
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.03.034
TI - Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling
T2 - Mendeleev Communications
AU - Matyugina, Elena Sergeevna
AU - Khandazhinskaya, Anastasia Lvovna
AU - Kochetkov, Sergei Nikolaevich
AU - Seley-Radtke, Katherine L
PY - 2020
DA - 2020/03/02
PB - Mendeleev Communications
SP - 231-232
IS - 2
VL - 30
ER -
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@article{2020_Matyugina,
author = {Elena Sergeevna Matyugina and Anastasia Lvovna Khandazhinskaya and Sergei Nikolaevich Kochetkov and Katherine L Seley-Radtke},
title = {Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling},
journal = {Mendeleev Communications},
year = {2020},
volume = {30},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.03.034},
number = {2},
pages = {231--232},
doi = {10.1016/j.mencom.2020.03.034}
}
MLA
Cite this
MLA Copy
Matyugina, Elena Sergeevna, et al. “Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling.” Mendeleev Communications, vol. 30, no. 2, Mar. 2020, pp. 231-232. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.03.034.

Keywords

fleximers
heterocyclic aromatic compounds
iodination
Pyrrole
silyl protection
Suzuki–Miyaura cross-coupling

Abstract

1-[tert-Butyl(diphenyl)silyl]pyrrol-3-ylboronic acid was obtained from pyrrole in three steps. Its Suzuki–Miyaura cross-coupling with functionalized pyridinyl and pyrimidinyl bromides afforded new promising 3-hetaryl-1H-pyrroles.

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