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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| Médium: | Статья |
| Jazyk: | English |
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Royal Society of Chemistry
2018
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| On-line přístup: | 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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