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Ring Lithiation of 1,8-Bis(dimethylamino)naphthalene: Another Side of the ‘Proton Sponge Coin’. / Antonov, Alexander S.; Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Suponitsky, Kyrill Yu.; Tolstoy, Peter M.; Vovk, Mikhail A.

в: Dalton Transactions, Том 44, № 49, 2015, стр. 17756-17766.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Antonov, AS, Pozharskii, AF, Ozeryanskii, VA, Filarowski, A, Suponitsky, KY, Tolstoy, PM & Vovk, MA 2015, 'Ring Lithiation of 1,8-Bis(dimethylamino)naphthalene: Another Side of the ‘Proton Sponge Coin’', Dalton Transactions, Том. 44, № 49, стр. 17756-17766. https://doi.org/10.1039/C5DT02482J, https://doi.org/10.1039/c5dt02482j

APA

Antonov, A. S., Pozharskii, A. F., Ozeryanskii, V. A., Filarowski, A., Suponitsky, K. Y., Tolstoy, P. M., & Vovk, M. A. (2015). Ring Lithiation of 1,8-Bis(dimethylamino)naphthalene: Another Side of the ‘Proton Sponge Coin’. Dalton Transactions, 44(49), 17756-17766. https://doi.org/10.1039/C5DT02482J, https://doi.org/10.1039/c5dt02482j

Vancouver

Author

Antonov, Alexander S. ; Pozharskii, Alexander F. ; Ozeryanskii, Valery A. ; Filarowski, Aleksander ; Suponitsky, Kyrill Yu. ; Tolstoy, Peter M. ; Vovk, Mikhail A. / Ring Lithiation of 1,8-Bis(dimethylamino)naphthalene: Another Side of the ‘Proton Sponge Coin’. в: Dalton Transactions. 2015 ; Том 44, № 49. стр. 17756-17766.

BibTeX

@article{dbecadda71554f5faeef62a4fe6d436c,
title = "Ring Lithiation of 1,8-Bis(dimethylamino)naphthalene: Another Side of the {\textquoteleft}Proton Sponge Coin{\textquoteright}",
abstract = "It has been found that 1,8-bis(dimethylamino)naphthalene (DMAN), unlike N,N-dimethylaniline, undergoes ring metallation in the n-BuLi–TMEDA–Et2O system with a low selectivity and in poor total yields. The situation is significantly improved in the t-BuLi–TMEDA–n-hexane system when 3- and 4-lithium derivatives become the only reaction products obtained in good yields. The formation of 3-Li-DMAN is especially desired since no method of direct meta-functionalization of DMAN is known to date. The relative stability and structure of DMAN lithium derivatives have been examined with the help of X-ray and multinuclear NMR measurements as well as DFT calculations.",
keywords = "Спектроскопия ЯМР, протонные губки",
author = "Antonov, {Alexander S.} and Pozharskii, {Alexander F.} and Ozeryanskii, {Valery A.} and Aleksander Filarowski and Suponitsky, {Kyrill Yu.} and Tolstoy, {Peter M.} and Vovk, {Mikhail A.}",
year = "2015",
doi = "10.1039/C5DT02482J",
language = "English",
volume = "44",
pages = "17756--17766",
journal = "Dalton Transactions",
issn = "1477-9226",
publisher = "Royal Society of Chemistry",
number = "49",

}

RIS

TY - JOUR

T1 - Ring Lithiation of 1,8-Bis(dimethylamino)naphthalene: Another Side of the ‘Proton Sponge Coin’

AU - Antonov, Alexander S.

AU - Pozharskii, Alexander F.

AU - Ozeryanskii, Valery A.

AU - Filarowski, Aleksander

AU - Suponitsky, Kyrill Yu.

AU - Tolstoy, Peter M.

AU - Vovk, Mikhail A.

PY - 2015

Y1 - 2015

N2 - It has been found that 1,8-bis(dimethylamino)naphthalene (DMAN), unlike N,N-dimethylaniline, undergoes ring metallation in the n-BuLi–TMEDA–Et2O system with a low selectivity and in poor total yields. The situation is significantly improved in the t-BuLi–TMEDA–n-hexane system when 3- and 4-lithium derivatives become the only reaction products obtained in good yields. The formation of 3-Li-DMAN is especially desired since no method of direct meta-functionalization of DMAN is known to date. The relative stability and structure of DMAN lithium derivatives have been examined with the help of X-ray and multinuclear NMR measurements as well as DFT calculations.

AB - It has been found that 1,8-bis(dimethylamino)naphthalene (DMAN), unlike N,N-dimethylaniline, undergoes ring metallation in the n-BuLi–TMEDA–Et2O system with a low selectivity and in poor total yields. The situation is significantly improved in the t-BuLi–TMEDA–n-hexane system when 3- and 4-lithium derivatives become the only reaction products obtained in good yields. The formation of 3-Li-DMAN is especially desired since no method of direct meta-functionalization of DMAN is known to date. The relative stability and structure of DMAN lithium derivatives have been examined with the help of X-ray and multinuclear NMR measurements as well as DFT calculations.

KW - Спектроскопия ЯМР

KW - протонные губки

U2 - 10.1039/C5DT02482J

DO - 10.1039/C5DT02482J

M3 - Article

VL - 44

SP - 17756

EP - 17766

JO - Dalton Transactions

JF - Dalton Transactions

SN - 1477-9226

IS - 49

ER -

ID: 3977118