The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid | Sciact - CRIS-система Института катализа

The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid Научная публикация

Журнал

Helvetica Chimica Acta
ISSN: 0018-019X , E-ISSN: 1522-2675

Вых. Данные

Год: 2015, Том: 98, Номер: 10, Страницы: 1442-1455 Страниц : 14 DOI: 10.1002/hlca.201500125

Ключевые слова

Acid metabolites, Antiparkinsonian activity, Isomerization, Monoterpenoids, Oxidation

Авторы

Ardashov Oleg V. ^1,2 , Demidova Yuliya S. ^2,3 , Korchagina Dina V. ¹ , Volcho Konstantin P. ^1,2 , Simakova Irina L. ^2,3 , Salakhutdinov Nariman F. ^1,2

Организации

1	Novosibirsk Institute of Organic Chemistry, pr. Lavrentieva, 9, RU-630090 Novosibirsk
2	Novosibirsk State University, Pirogova 2, RU-630090 Novosibirsk
3	Boreskov Institute of Catalysis, pr. Lavrentieva, 5, RU-630090 Novosibirsk

Информация о финансировании (1)

Федеральное агентство научных организаций России

V.46.4.4.

A putative acid metabolite of a novel highly effective antiparkinsonian agent, (4S,5R,6R)-5,6-dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid (5), was synthesized for the first time. Several synthetic approaches based on different transformations of O-bearing monoterpenoids of the pinane and p-menthane series were developed and tested in the course of the study. Acid 5 was synthesized starting from a commercially available monoterpenoid, (−)-verbenone, in a total yield of 4.4% over eight steps.

Ardashov O.V. , Demidova Y.S. , Korchagina D.V. , Volcho K.P. , Simakova I.L. , Salakhutdinov N.F.
The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid
Helvetica Chimica Acta. 2015. V.98. N10. P.1442-1455. DOI: 10.1002/hlca.201500125 WOS Scopus РИНЦ CAPlusCA OpenAlex

Поступила в редакцию:	19 мая 2015 г.
Опубликована в печати:	1 окт. 2015 г.
Опубликована online:	13 окт. 2015 г.

Web of science:	WOS:000362958200013
Scopus:	2-s2.0-84943791180
РИНЦ:	24960801
Chemical Abstracts:	2015:1657478
Chemical Abstracts (print):	163:618121
OpenAlex:	W1945098908

БД	Цитирований
Web of science	5
Scopus	7
РИНЦ	7
OpenAlex	6