Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with alpha-amino acid derivatives Научная публикация
| Журнал |
Steroids
ISSN: 0039-128X , E-ISSN: 1878-5867 |
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| Вых. Данные | Год: 2017, Том: 117, Номер: SI, Страницы: 112-119 Страниц : 8 DOI: 10.1016/j.steroids.2016.09.016 | ||||
| Ключевые слова | Amino acids; (+)-3-Carene; (-)-alpha-Pinene; Nitroso chlorides; Diastereoselectivity | ||||
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Реферат:
Reaction of nitrosochlorides of natural monoterpene hydrocarbons (+)-3-carene and (-)-alpha-pinene with L-amino acids and their methyl esters results in stereoselective formation of terpene-amino acids hybrids, which belong to the series of alpha-substituted amino oximes. The reaction with an excess of racemic DL-amino acids and their derivatives induces partial resolution of the amino acid components and formation of the diastereomeric mixtures of the terpene-amino acids hybrids, with diastereomeric excess varying from 0 to 100%. (C) 2016 Elsevier Inc. All rights reserved.
Библиографическая ссылка:
Marenin K.S.
, Gatilov Y.V.
, Agafontsev A.M.
, Tkachev A.V.
Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with alpha-amino acid derivatives
Steroids. 2017. V.117. NSI. P.112-119. DOI: 10.1016/j.steroids.2016.09.016 WOS Scopus РИНЦ OpenAlex
Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with alpha-amino acid derivatives
Steroids. 2017. V.117. NSI. P.112-119. DOI: 10.1016/j.steroids.2016.09.016 WOS Scopus РИНЦ OpenAlex
Даты:
| Опубликована в печати: | 1 янв. 2017 г. |
Идентификаторы БД:
| Web of science: | WOS:000392566800016 |
| Scopus: | 2-s2.0-85006753312 |
| РИНЦ: | 29466566 |
| OpenAlex: | W2526253820 |