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


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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.

About the authors

G. E. Salnikov

Novosibirsk Institute of Organic Chemistry, Siberian Branch; Novosibirsk State University

Email: koltunov@catalysis.ru
Russian Federation, Novosibirsk; Novosibirsk

A. M. Genaev

Novosibirsk Institute of Organic Chemistry, Siberian Branch

Email: koltunov@catalysis.ru
Russian Federation, Novosibirsk

A. V. Shernyukov

Novosibirsk Institute of Organic Chemistry, Siberian Branch; Novosibirsk State University

Email: koltunov@catalysis.ru
Russian Federation, Novosibirsk; Novosibirsk

Z. Zhu

Novosibirsk State University

Email: koltunov@catalysis.ru
Russian Federation, Novosibirsk

N. V. Tkachenko

Novosibirsk State University; Institute of Catalysis, Siberian Branch

Email: koltunov@catalysis.ru
Russian Federation, Novosibirsk; pr. Akademika Lavrent’eva 5, Novosibirsk, 630090

K. Yu. Koltunov

Novosibirsk State University; Institute of Catalysis, Siberian Branch

Author for correspondence.
Email: koltunov@catalysis.ru
Russian Federation, Novosibirsk; pr. Akademika Lavrent’eva 5, Novosibirsk, 630090

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