Three-component synthesis of functionalized 5-oxo-4,5-dihydroindeno[1,2-b]pyrans.
Issa Yavari, Mehdi Sirouspour, Sanaz Souri
Index: Mol. Divers. 10(2) , 265-70, (2006)
Full Text: HTML
Abstract
Protonation of the reactive intermediates produced in the reaction between alkyl(aryl) isocyanides and dialkyl acetylenedicarboxylates by indan-1,3-dione leads to vinylnitrilium cations, which undergo carbon centered Michael type addition with the conjugate base of the CH-acid to produce functionalized 5-oxo-4,5-dihydroindeno[1,2-b]pyrans.
Related Compounds
Related Articles:
2013-02-01
[Mol. Divers. 17(1) , 55-61, (2013)]
2011-12-15
[Bioorg. Med. Chem. Lett. 21 , 7273-6, (2011)]
2010-09-17
[J. Org. Chem. 75(18) , 6244-51, (2010)]
2006-05-01
[Mol. Divers. 10(2) , 247-50, (2006)]
2012-02-01
[Mol. Divers. 16(1) , 145-50, (2012)]