Investigation of the Diastomerism of Compounds with a Long-Chain Tether between the Stereogenic Centers Full article
Journal |
Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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Output data | Year: 2019, Volume: 55, Number: 2, Pages: 161-167 Pages count : 7 DOI: 10.1134/s1070428019020064 | ||||
Tags | NMR, podand diastereomerism, oxazolopyridines, pyramidal nitrogen inversion, secondary helical structure of the hydroxyethyl chain | ||||
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Abstract:
The NMR spectra of several heterocyclic compounds synthesized at Omsk universities revealed manifestation of a diasteomerism at a large (up to fifteen bonds) distance between the stereogenic centers. This phenomenon was explained by a regular helical secondary structure of the tether between the centers.
Cite:
Talsi V.P.
, Evdokimov S.N.
, Shatsauskas A.L.
Investigation of the Diastomerism of Compounds with a Long-Chain Tether between the Stereogenic Centers
Russian Journal of Organic Chemistry. 2019. V.55. N2. P.161-167. DOI: 10.1134/s1070428019020064 WOS Scopus РИНЦ
Investigation of the Diastomerism of Compounds with a Long-Chain Tether between the Stereogenic Centers
Russian Journal of Organic Chemistry. 2019. V.55. N2. P.161-167. DOI: 10.1134/s1070428019020064 WOS Scopus РИНЦ
Original:
Талзи В.П.
, Евдокимов С.Н.
, Шацаускас А.Л.
Исследование диастеомерии соединений, в которых стереогенные центры разделены длинной цепью
Журнал органической химии. 2019. №2. С.208-214. DOI: 10.1134/S051474921902006X РИНЦ
Исследование диастеомерии соединений, в которых стереогенные центры разделены длинной цепью
Журнал органической химии. 2019. №2. С.208-214. DOI: 10.1134/S051474921902006X РИНЦ
Dates:
Submitted: | Aug 31, 2018 |
Accepted: | Sep 10, 2018 |
Published print: | Feb 1, 2019 |
Published online: | Apr 23, 2019 |
Identifiers:
Web of science | WOS:000465521400006 |
Scopus | 2-s2.0-85064731887 |
Elibrary | 38675559 |
OpenAlex | W2940450122 |
Citing:
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