1292288-53-9Relevant academic research and scientific papers
A novel, chemoselective one-pot procedure for the preparation of 3H-spiro[isobenzofuran-1,2′-pyrrole]-3,3′(1′H)-dione derivatives via oxidative cleavage of 3a,8b-dihydroxyindeno[1,2-b]pyrroles
Mahdavinia, Gholam Hossein,Mohammadizadeh, Mohammad R.,Ariapour, Noushin,Alborz, Maryam
, p. 1967 - 1970 (2014/04/03)
A one-pot, efficient and chemoselective procedure for the synthesis of new 3H-spiro[isobenzofuran-1,2′-pyrrole]-3,3′(1′H)-dione derivatives has been developed which involves room temperature oxidative cleavage of 3a,8b-dihydroxyindeno[1,2-b]pyrroles themselves synthesized from the reaction of ninhydrin and enaminones in 30% ethanol. A reasonable mechanism is proposed for the oxidation reaction based on the results of this study and our previous related work.
Efficient and chemoselective methods for the synthesis of some isobenzofuran and spiro[isobenzofuran-1,2′-pyrrole] derivatives
Mohammadizadeh, Mohammad R.,Firoozi, Neda,Aradeh
experimental part, p. 410 - 416 (2011/04/26)
An efficient and practical one-pot procedure for the direct chemoselective synthesis of isobenzofuran and spiro[isobenzofuran-1,2′-pyrrole] derivatives is developed via oxidative cleavage of 3a,8b-dihydroxyindeno[1,2-b] pyrrol-4-ones with Pb(OAc)4/s
