Oxidative coupling of tetraalkynyltin with aldehydes leading to alkynyl ketones

The reaction of tetraalkynyltin with aldehydes was studied for the first time. The reaction was shown to proceed as a tandem process of nucleophilic addition of tin acetylide to aldehyde followed by Oppenauer-type oxidation of produced tin alcoholates, and may be used as a convenient one-pot approach to acetylenic ketones. The advantages and limitations of the proposed method are discussed. © 2017 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

Авторы
Levashov A.S.1 , Aksenov N.A. 2, 3 , Aksenova I.V.2 , Konshin V.V.1
Издательство
Royal Society of Chemistry
Номер выпуска
16
Язык
Английский
Страницы
8297-8304
Статус
Опубликовано
Том
41
Год
2017
Организации
  • 1 Department of Organic Chemistry and Technologies, Kuban State University, 149 Stavropolskaya str., Krasnodar, 350040, Russian Federation
  • 2 Department of Chemistry, North Caucasus Federal University, 1a Pushkin str., Stavropol, 355009, Russian Federation
  • 3 Peoples Friendship University Russia, 6 Miklukho Maklaya St, Moscow, 117198, Russian Federation
Ключевые слова
aldehyde derivative; ketone derivative; stannic chloride; alkynylation; Article; catalyst; controlled study; hydrolysis; molecular weight; nucleophilicity; oxidation; oxidative coupling; priority journal; solvation; synthesis; X ray diffraction
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6037/
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