Palladium (II)-catalysed intramolecular C–H functionalizations: Efficient synthesis of kealiinine C and analogues

An efficient palladium-catalysed C–H functionalization sequence has been developed for the synthesis of 2-aminoimidazole alkaloids (Kealiinine C) and its analogues. This protocol proceeds via iodocyclisation of propargylguanidines followed by intramolecular Pd-catalysed cyclisation. © 2018 Elsevier B.V.

Авторы
Saha D.1, 3 , Stolarzewicz I.1 , Bahadur V.1, 2 , Sharma U.K.1 , Voskressensky L.G. 4 , Sharma A.3 , Singh B.K.2 , Van Der Eycken E.V.
Журнал
Molecular Catalysis
Издательство
Elsevier B.V.
Язык
Английский
Страницы
233-238
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.1016/j.mcat.2018.06.007
Том
455
Год
2018
Организации
  • 1 Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, Leuven, B-3001, Belgium
  • 2 Bioorganic Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India
  • 3 Medicinal Chemistry Lab, Department of Chemistry, Indian Institute of Technology Roorkee, Uttarakhand, 247667, India
  • 4 Peoples Friendship University of Russia (RUDN University), Miklukho-Maklaya Street 6, Moscow, 117198, Russian Federation
Ключевые слова
2-aminoimidazoles; C–H functionalization; Guanylation; Iodocyclization; Kealiinines
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6496/
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