Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines

Highly efficient spiro-condensation enabling cyclic enoles to act as 1,3-bis-nucleophiles in reaction with pyrrole-2,3-diones acting as 1,2-bis-electrophiles was developed. The corresponding furo[3,2-c]coumarins and furo[3,2-c]quinolines containing a spiro pyrrole fragment were obtained in high yiel...

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Главные авторы:	Rubin, M. A., Рубин, М. А.
Формат:	Статья
Язык:	English
Опубликовано:	Royal Society of Chemistry 2018
Темы:	Condensation High yield Aromatic compounds
Online-ссылка:	https://www.scopus.com/record/display.uri?eid=2-s2.0-84987617593&origin=resultslist&sort=plf-f&src=s&st1=Spiro-condensation+of+5-methoxycarbonyl-1%3a+H+-pyrrole-2%2c3-diones+with+cyclic+enoles+to+form+spiro+substituted+furo%5b3%2c2-+c%5d+-coumarins+and+quinolines&st2=&sid=31d5f356b1316242306d1d2965b7258d&sot=b&sdt=b&sl=163&s=TITLE-ABS-KEY%28Spiro-condensation+of+5-methoxycarbonyl-1%3a+H+-pyrrole-2%2c3-diones+with+cyclic+enoles+to+form+spiro+substituted+furo%5b3%2c2-+c%5d+-coumarins+and+quinolines%29&relpos=0&citeCnt=4&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/3458
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record_format	dspace
spelling	ir-20.500.12258-34582020-07-31T09:56:40Z Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines Rubin, M. A. Рубин, М. А. Condensation High yield Aromatic compounds Highly efficient spiro-condensation enabling cyclic enoles to act as 1,3-bis-nucleophiles in reaction with pyrrole-2,3-diones acting as 1,2-bis-electrophiles was developed. The corresponding furo[3,2-c]coumarins and furo[3,2-c]quinolines containing a spiro pyrrole fragment were obtained in high yields 2018-11-20T14:29:35Z 2018-11-20T14:29:35Z 2016 Статья Dubovtsev, A.Yu., Silaichev, P.S., Nazarov, M.A., Dmitriev, M.V., Maslivets, A.N., Rubin, M. Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines // RSC Advances. - 2016. - Volume 6. - Issue 88. - Pages 84730-84737 https://www.scopus.com/record/display.uri?eid=2-s2.0-84987617593&origin=resultslist&sort=plf-f&src=s&st1=Spiro-condensation+of+5-methoxycarbonyl-1%3a+H+-pyrrole-2%2c3-diones+with+cyclic+enoles+to+form+spiro+substituted+furo%5b3%2c2-+c%5d+-coumarins+and+quinolines&st2=&sid=31d5f356b1316242306d1d2965b7258d&sot=b&sdt=b&sl=163&s=TITLE-ABS-KEY%28Spiro-condensation+of+5-methoxycarbonyl-1%3a+H+-pyrrole-2%2c3-diones+with+cyclic+enoles+to+form+spiro+substituted+furo%5b3%2c2-+c%5d+-coumarins+and+quinolines%29&relpos=0&citeCnt=4&searchTerm= http://hdl.handle.net/20.500.12258/3458 en RSC Advances application/pdf application/pdf Royal Society of Chemistry
institution	СКФУ
collection	Репозиторий
language	English
topic	Condensation High yield Aromatic compounds
spellingShingle	Condensation High yield Aromatic compounds Rubin, M. A. Рубин, М. А. Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
description	Highly efficient spiro-condensation enabling cyclic enoles to act as 1,3-bis-nucleophiles in reaction with pyrrole-2,3-diones acting as 1,2-bis-electrophiles was developed. The corresponding furo[3,2-c]coumarins and furo[3,2-c]quinolines containing a spiro pyrrole fragment were obtained in high yields
format	Статья
author	Rubin, M. A. Рубин, М. А.
author_facet	Rubin, M. A. Рубин, М. А.
author_sort	Rubin, M. A.
title	Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
title_short	Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
title_full	Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
title_fullStr	Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
title_full_unstemmed	Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
title_sort	spiro-condensation of 5-methoxycarbonyl-1: h -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines
publisher	Royal Society of Chemistry
publishDate	2018
url	https://www.scopus.com/record/display.uri?eid=2-s2.0-84987617593&origin=resultslist&sort=plf-f&src=s&st1=Spiro-condensation+of+5-methoxycarbonyl-1%3a+H+-pyrrole-2%2c3-diones+with+cyclic+enoles+to+form+spiro+substituted+furo%5b3%2c2-+c%5d+-coumarins+and+quinolines&st2=&sid=31d5f356b1316242306d1d2965b7258d&sot=b&sdt=b&sl=163&s=TITLE-ABS-KEY%28Spiro-condensation+of+5-methoxycarbonyl-1%3a+H+-pyrrole-2%2c3-diones+with+cyclic+enoles+to+form+spiro+substituted+furo%5b3%2c2-+c%5d+-coumarins+and+quinolines%29&relpos=0&citeCnt=4&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/3458
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Spiro-condensation of 5-methoxycarbonyl-1: H -pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2- c] -coumarins and quinolines

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