1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene

1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene Научная публикация

Журнал

Mendeleev Communications
ISSN: 0959-9436

Вых. Данные

Год: 2019, Том: 29, Номер: 1, Страницы: 53-54 Страниц : 2 DOI: 10.1016/j.mencom.2019.01.016

Авторы

Budaev Arsalan B. ¹ , Ivanov Andrei V. ¹ , Petrova Olga V. ¹ , Samsonov Vladimir A. ² , Ushakov Igor A. ¹ , Tikhonov Aleksei Ya. ² , Sobenina Lyubov N. ¹ , Trofimov Boris A. ¹

Организации

1	(Данные Web of science) Russian Acad Sci, Siberian Branch, AE Favorsky Irkutsk Inst Chem, Irkutsk 664033, Russia
2	(Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

6,7-Dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime is annelated with acetylene in the KOH/DMSO/H2O system under pressure to give NH- or N-vinyl-5,8-dihydro-4H-[1,2,5]-oxadiazolo[3,4-g]indoles in 29 and 68% yields, respectively. These derivatives are readily aromatized with DDQ at room temperature to the expected indoles.

Budaev A.B. , Ivanov A.V. , Petrova O.V. , Samsonov V.A. , Ushakov I.A. , Tikhonov A.Y. , Sobenina L.N. , Trofimov B.A.
1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
Mendeleev Communications. 2019. V.29. N1. P.53-54. DOI: 10.1016/j.mencom.2019.01.016 WOS Scopus РИНЦ

Опубликована в печати:

1 янв. 2019 г.

Web of science	WOS:000460711400016
Scopus	2-s2.0-85061594776
РИНЦ	38668546
OpenAlex	W2913656493