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First synthesis of p-mentha-1,8-diene triol Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2013, Volume: 62, Number: 1, Pages: 171-174 Pages count : DOI: 10.1007/s11172-013-0025-1
Tags p-mentha-1,8-dienes; triols; epoxides; verbenone; isomerisation
Authors Ardashov O. V. 1 , Khaid E. V. 2 , Mikhal'chenko O. S. 1 , Korchagina D. V. 1 , Volcho K. P. 1 , Salakhutdinov N. F. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Abstract: The first synthesis of p-mentha-1,8-diene triol from (-)-verbenone included obtaining pinane epoxy diol and its subsequent acid-catalyzed rearrangement on montmorillonite clay as the key steps.
Cite: Ardashov O.V. , Khaid E.V. , Mikhal'chenko O.S. , Korchagina D.V. , Volcho K.P. , Salakhutdinov N.F.
First synthesis of p-mentha-1,8-diene triol
Russian Chemical Bulletin. 2013. V.62. N1. P.171-174. DOI: 10.1007/s11172-013-0025-1 WOS Scopus РИНЦ OpenAlex
Original: Ардашов О.В. , Хаид Е.В. , Патрушева О.С. , Корчагина Д.В. , Волчо К.П. , Салахутдинов Н.Ф.
Первый синтез n-мента-1,8-диенового триола
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2013. №1. С.172. РИНЦ
Dates:
Published print: Jan 1, 2013
Published online: Jan 11, 2014
Identifiers:
Web of science: WOS:000326095300025
Scopus: 2-s2.0-84887126114
Elibrary: 21887579
OpenAlex: W2067948502
Citing:
DB Citing
Web of science 5
Scopus 5
Elibrary 6
OpenAlex 5
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