Michael addition of ethyl acetoacetate to alpha,beta-unsaturated oximes in the presence of FeCl3: a novel synthetic route to substituted nicotinic acid derivatives Научная публикация
| Журнал |
Tetrahedron Letters
ISSN: 0040-4039 |
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| Вых. Данные | Год: 2000, Том: 41, Номер: 41, Страницы: 8011-8013 Страниц : DOI: 10.1016/S0040-4039(00)01391-5 | ||||||
| Ключевые слова | Michael addition; iron(III) chloride hexahydrate; unsaturated oxime; nicotinic acid | ||||||
| Авторы |
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Реферат:
The FeCl3-catalyzed reaction of alpha,beta-unsaturated oximes with ethyl acetoacetate resulted in Michael addition followed by ring closure to produce substituted nicotinic acid derivatives in a very efficient way. (C) 2000 Elsevier Science Ltd. All rights reserved.
Библиографическая ссылка:
Chibiryaev A.
, De Kimpe N.
, Tkachev A.
Michael addition of ethyl acetoacetate to alpha,beta-unsaturated oximes in the presence of FeCl3: a novel synthetic route to substituted nicotinic acid derivatives
Tetrahedron Letters. 2000. V.41. N41. P.8011-8013. DOI: 10.1016/S0040-4039(00)01391-5 WOS Scopus OpenAlex
Michael addition of ethyl acetoacetate to alpha,beta-unsaturated oximes in the presence of FeCl3: a novel synthetic route to substituted nicotinic acid derivatives
Tetrahedron Letters. 2000. V.41. N41. P.8011-8013. DOI: 10.1016/S0040-4039(00)01391-5 WOS Scopus OpenAlex
Даты:
| Опубликована в печати: | 1 окт. 2000 г. |
Идентификаторы БД:
| Web of science: | WOS:000089809800049 |
| Scopus: | 2-s2.0-0034619162 |
| OpenAlex: | W2033125110 |