• Single molecules put a ring on it. Sarah E. Riesman, News and Views, Nature, 2012, 490, 179.
• Renewed focus on a neglected reaction. Chemical & Engineering News, 90 (42), October 15, 2012.
• “A Hot, Energized” Benzyne. Reinhard W. Hoffmann and Keisuke Suzuki, Angewandte Chemie International Edition Highlights, 2013, 52, 2655.
• The Hexadehydro-Diels-Alder Reaction-A New Method Yielding Benzenoids. Synfacts, 2013, 9(2), 0153.
• Drei mal drei, Michael Groß, Chem. Unserer Zeit, 2012, 46.
• Turbo-charged Diels-Alder reaction. Ian Le Guillou, Chemistry World.
• A new Diels-Alder reaction, Derek Lowe, Pipeline.
• The Hexadehydro-Diels-Alder Reaction: A New Chapter in Aryne Chemistry. Catherine Holden (née Hall) and Prof. Michael F. Greaney, Angewandte Chemie International Edition Highlights, 2014, 53, 5746.
• https://en.wikipedia.org/wiki/ Hexadehydro Diels-Alder_reaction.
• Formal Total Synthesis of Selaginpulvilin D. Bhavani Shankar Chinta and Beeraiah Baire*, Org. Biomol. Chem., 2017, 15, 5908-5911. (Featured as a cover page)
• The Z-enoate assisted, Meyer–Schuster rearrangement cascade: unconventional synthesis of α-arylenone esters. Prabhakararao Tharra and Beeraiah Baire, Chem. Commun., 2016, 52, 12147-12150. (Featured as a cover page)
• Mild Approach to 2-acylfurans via Intercepted Meyer-Schuster rearrangement of 6-hydroxyhex-2-en-4-ynals. Prabhakara rao Tharra and Beeraiah Baire, J. Org. Chem., 2015, 80 (16), 8314–8328. was highlighted in Organic Chemistry Highlights June 2016.