Inside Cover Picture: Rhodium(III)‐Catalyzed, CH Activated Annulation to Form Isocoumarins and α‐Pyrones using the ON Bond as an Internal Oxidant (Adv. Synth. Catal. 7/2014). Issue 7 (24th April 2014)

• Record Type: Journal Article
• Authors: Li, Xing Guang; Liu, Kai; Zou, Gang; Liu, Pei Nian
• Is Part Of: Advanced synthesis & catalysis. Volume 356:Issue 7(2014)
• Page Start: 1382
• Page End: 1382
• Publication Date: 2014-04-24
• Subjects: Catalysis -- Periodicals; Organic compounds -- Synthesis -- Periodicals; Chemistry -- Periodicals; Chemistry, Technical -- Periodicals; Chemistry -- Periodicals; Catalysis -- Periodicals; Technology, Pharmaceutical -- Periodicals; 547.2
• DOI: 10.1002/adsc.201400366
• Languages: English
• ISSNs: 1615-4150

Abstract

<abstract abstract-type="graphical" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>The inside cover picture</bold>, provided by Pei Nian Liu and co‐workers, illustrates a mild and regioselective redox‐neutral CH activated annulation protocol for the synthesis of isocoumarins and <italic>α</italic>‐pyrones. Without any external oxidant, an ON bond was employed as the internal oxidant in the Rh(III)‐catalyzed annulation. This coupling of benzoates and alkynes is potentially applicable to construct of a broad range of useful O‐heterocycles. Details are reported in the Communication on <ext-link ext-link-type="doi" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">pages 1496–1500 (X. G. Li, K. Liu, G. Zou, P. N. Liu, Adv. Synth. Catal.­ 2014, 356, 1496–1500; DOI: 10.1002/adsc.201400200)</ext-link>.<boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh5bwfvg" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract>