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Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF. / Salnikov, G. E.; Genaev, A. M.; Shernyukov, A. V. et al.

In: Russian Journal of Organic Chemistry, Vol. 54, No. 5, 01.05.2018, p. 792-794.

Research output: Contribution to journal › Article › peer-review

Harvard

Salnikov, GE, Genaev, AM, Shernyukov, AV, Zhu, Z, Tkachenko, NV & Koltunov, KY 2018, 'Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF', Russian Journal of Organic Chemistry, vol. 54, no. 5, pp. 792-794. https://doi.org/10.1134/S1070428018050214

APA

Salnikov, G. E., Genaev, A. M., Shernyukov, A. V., Zhu, Z., Tkachenko, N. V., & Koltunov, K. Y. (2018). Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF. Russian Journal of Organic Chemistry, 54(5), 792-794. https://doi.org/10.1134/S1070428018050214

Vancouver

Salnikov GE, Genaev AM, Shernyukov AV, Zhu Z, Tkachenko NV, Koltunov KY. Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF. Russian Journal of Organic Chemistry. 2018 May 1;54(5):792-794. doi: 10.1134/S1070428018050214

Author

Salnikov, G. E. ; Genaev, A. M. ; Shernyukov, A. V. et al. / Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF. In: Russian Journal of Organic Chemistry. 2018 ; Vol. 54, No. 5. pp. 792-794.

BibTeX

@article{45976061648647408faa4b663804baa1,
title = "Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF",
abstract = "Although 1,1′-bi-2-naphthol (BINOL) is known to racemize in aqueous mineral acids and much more readily in superacids, it retains its initial configuration in one of the strongest superacid system, HSO3F-SbF5-SO2ClF due to protective C8,C8′-diprotonation.",
author = "Salnikov, {G. E.} and Genaev, {A. M.} and Shernyukov, {A. V.} and Z. Zhu and Tkachenko, {N. V.} and Koltunov, {K. Yu}",
note = "Publisher Copyright: {\textcopyright} 2018, Pleiades Publishing, Ltd.",
year = "2018",
month = may,
day = "1",
doi = "10.1134/S1070428018050214",
language = "English",
volume = "54",
pages = "792--794",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "5",

}

RIS

TY - JOUR

T1 - Configurational Stability of 1,1′-Bi-2-naphthol in Superacid System HSO3F–SbF5–SO2ClF

AU - Salnikov, G. E.

AU - Genaev, A. M.

AU - Shernyukov, A. V.

AU - Zhu, Z.

AU - Tkachenko, N. V.

AU - Koltunov, K. Yu

N1 - Publisher Copyright: © 2018, Pleiades Publishing, Ltd.

PY - 2018/5/1

Y1 - 2018/5/1

N2 - Although 1,1′-bi-2-naphthol (BINOL) is known to racemize in aqueous mineral acids and much more readily in superacids, it retains its initial configuration in one of the strongest superacid system, HSO3F-SbF5-SO2ClF due to protective C8,C8′-diprotonation.

AB - Although 1,1′-bi-2-naphthol (BINOL) is known to racemize in aqueous mineral acids and much more readily in superacids, it retains its initial configuration in one of the strongest superacid system, HSO3F-SbF5-SO2ClF due to protective C8,C8′-diprotonation.

UR - http://www.scopus.com/inward/record.url?scp=85049154732&partnerID=8YFLogxK

U2 - 10.1134/S1070428018050214

DO - 10.1134/S1070428018050214

M3 - Article

AN - SCOPUS:85049154732

VL - 54

SP - 792

EP - 794

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 5

ER -

ID: 14277573