caa a22 4500 605529825 CHVBK 20210128100820.0 cr unu---uuuuu 210128e20151001xx s 000 0 eng 10.1134/S1070428015100012 doi (NATIONALLICENCE)springer-10.1134/S1070428015100012 Reaction of monoterpene hydroxy thiols with chlorine dioxide [Elektronische Daten] [O. Lezina, O. Grebenkina, D. Sudarikov, Yu. Krymskaya, S. Rubtsova, A. Kutchin] Reactions of isobornane and pinane hydroxy thiols with chlorine dioxide have been studied. Unlike pinane derivatives, hydroxy thiols of the isobornane series reacted with chlorine dioxide to give the corresponding sulfinyl derivatives with high stereoselectivity. New terpenoids containing sulfur, oxygen, and chlorine atoms have been synthesized by oxidation of hydroxy thiols with chlorine dioxide. Pleiades Publishing, Ltd., 2015 Lezina O. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut Grebenkina O. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut Sudarikov D. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut Krymskaya Yu Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut Rubtsova S. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut Kutchin A. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut Russian Journal of Organic Chemistry Pleiades Publishing 51/10(2015-10-01), 1359-1367 1070-4280 51:10<1359 2015 51 11178 https://doi.org/10.1134/S1070428015100012 text/html Onlinezugriff via DOI BK010053 XK010053 XK010000 Metadata rights reserved Springer special CC-BY-NC licence nationallicence 1 research-article jats NATIONALLICENCE NATIONALLICENCE NL-springer NATIONALLICENCE 856 40 https://doi.org/10.1134/S1070428015100012 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Lezina O. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut NATIONALLICENCE 700 1- Grebenkina O. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut NATIONALLICENCE 700 1- Sudarikov D. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut NATIONALLICENCE 700 1- Krymskaya Yu Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut NATIONALLICENCE 700 1- Rubtsova S. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut NATIONALLICENCE 700 1- Kutchin A. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia aut NATIONALLICENCE 773 0- Russian Journal of Organic Chemistry Pleiades Publishing 51/10(2015-10-01), 1359-1367 1070-4280 51:10<1359 2015 51 11178