{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T20:32:15Z","timestamp":1777494735214,"version":"3.51.4"},"reference-count":47,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2015,12,23]],"date-time":"2015-12-23T00:00:00Z","timestamp":1450828800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Eur J Org Chem"],"published-print":{"date-parts":[[2016,2]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Chiral 3\u2010amino\u20103\u2010aryloxindoles are important biologically active compounds. Using a catalytic modular approach, 31 new 3\u2010amino\u20103\u2010aryl\u20102\u2010oxindoles were prepared by a simple Rh\u2010catalysed addition of arylboronic acids to isatin\u2010derived <jats:italic>N<\/jats:italic>\u2010Boc\u2010protected ketimines (Boc = <jats:italic>tert\u2010<\/jats:italic>butoxycarbonyl). A low catalyst loading of 3 mol\u2010% was used, and the reaction showed a wide scope with high functional\u2010group compatibility, and gave good yields. We report the first catalytic enantioselective reactions with this substrate. Deprotection of the Boc group was easily accomplished in good yields.<\/jats:p>","DOI":"10.1002\/ejoc.201501399","type":"journal-article","created":{"date-parts":[[2015,12,23]],"date-time":"2015-12-23T13:26:48Z","timestamp":1450877208000},"page":"806-812","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":21,"title":["Modular Catalytic Synthesis of 3\u2010Amino\u20103\u2010aryl\u20102\u2010oxindoles: Rh Catalysis with Isatin\u2010Derived <i>N<\/i>\u2010Boc\u2010Protected Ketimines"],"prefix":"10.1002","volume":"2016","author":[{"given":"Carolina S.","family":"Marques","sequence":"first","affiliation":[]},{"given":"Anthony J.","family":"Burke","sequence":"additional","affiliation":[]}],"member":"311","published-online":{"date-parts":[[2015,12,23]]},"reference":[{"key":"e_1_2_6_1_2","first-page":"335","volume":"4","author":"Rudrangi S. R. S.","year":"2011","journal-title":"Asian J. Res. 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