Ag2O nanoparticle-catalyzed substrate-controlled regioselectivities: direct access to 3-ylidenephthalides and isocoumarins. Issue 41 (26th June 2018)

• Record Type: Journal Article
• Authors: Chaudhary, Sandeep; Shyamlal, Bharti Rajesh K.; Yadav, Lalit; Tiwari, Mohit K.; Kumar, Krishan
• Is Part Of: RSC advances. Volume 8:Issue 41(2018)
• Page Start: 23152
• Page End: 23162
• Publication Date: 2018-06-26
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c8ra03926g
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : We report the first example of an efficient, Ag2 O nanoparticle-catalyzed, direct regioselective synthesis of 3-ylidenephthalides and isocoumarins via Sonogashira type coupling followed by substrate-controlled 5- exo -dig or 6- endo -dig cyclization reaction, respectively. Abstract : Herein, we disclose the first example of an efficient, silver oxide nanoparticle-catalyzed, direct regioselective synthesis of 3-ylidenephthalides11–16 and isocoumarins17–20 via sonogashira type coupling followed by substrate-controlled 5- exo -dig or 6- endo -dig cyclization reaction, respectively. This one pot coupling involves reaction of substituted 2-halobenzoic acid with meta / para -substituted and ortho -substituted terminal alkynes, which proceeded in a regioselective manner resulting in the formation of 3-ylidenephthalides or isocoumarins, respectively, in excellent yields (up to 95%) with complete Z-selectivity. This protocol features relatively broad substrate scope, mild conditions, operational simplicity, and is favourable with aromatic/alicyclic terminal alkynes. The competition experiments and gram-scale synthesis further highlight the importance and versatility of the methodology. The proposed mechanistic pathways illustrate that the regioselectivity is substantially being controlled by the substituent(s) present on the acetylenic phenyl ring.