Step-by-Step Synthesis of Unsymmetrically Substituted Pyranoisocoumarins from Terephthalic Acid
Year: 2025
Type: article
Abstract: An efficient multi-step protocol for the selective synthesis of unsymmetrically substituted pyranoisocoumarins (pyrano[3,4-g]isochromene-1,6-diones) has been developed. The procedure includes the two-fold step-by-step C–H annulation of terephthalic acid with two different alkynes. The photophysical properties of pyranoisocoumarins were predicted by DFT calculations.
Source: INEOS OPEN
DOI: 10.32931/io2516a
Authors: M. A. Arsenov, A. V. Semenikhin, D. A. Loginov
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Awards: G116579644, G1530898836, G160288408
OpenAlex ID: W4412697995
