Synthesis, Table of Contents PAPER© Georg Thieme Verlag Stuttgart ˙ New YorkFriedel-Crafts Reactions of 2-Naphthol with α-Amido Sulfones and Conversion of the Products with Nucleophiles [¹] Biswanath Das*, Cheruku Ravindra Reddy, Chava Sindhu, Chithaluri Sudhakar, Siddavatam NagendraOrganic Chemistry Division-1, Indian Institute of Chemical Technology, Hyderabad 500 007, IndiaFax: +91(40)27193198; e-Mail: biswanathdas@yahoo.com; Recommend Article Abstract Buy Article All articles of this category Abstract 2-Naphthol underwent Friedel-Crafts reaction with N-benzyloxycarbonylamino sulfones in the presence of InCl3 at room temperature to form the corresponding sulfonyl derivatives in high yields. The products were subsequently reacted with nucleophiles such as allyltributyltin and anisole to replace the sulfonyl group. Key words 2-naphthol - α-amido sulfone - InCl3 - Friedel-Crafts reaction - nucleophile Full Text References References<A NAME="RZ17310SS-1">1</A> Part 209 in the series ‘Studies on Novel Synthetic Methodologies’. <A NAME="RZ17310SS-2">2</A> Shen AY. Tsai CT. Chen CL. Eur. J. Med Chem. 1999, 34: 877 <A NAME="RZ17310SS-3A">3a</A> Das B. Laxminarayana K. Ravikanth B. Rao BR. J. Mol. Catal. A: Chem. 2007, 261: 180 <A NAME="RZ17310SS-3B">3b</A> Das B. Veeranjaneyulu B. Krishnaiah M. Balasubramanyam P. Synth. Commun. 2009, 39: 1929 <A NAME="RZ17310SS-4A">4a</A> Khodaei MM. Khosropour AR. Moghanian H. Synlett 2006, 916 <A NAME="RZ17310SS-4B">4b</A> Selvam NP. Perumal PT. Tetrahedron Lett. 2006, 47: 7481 <A NAME="RZ17310SS-4C">4c</A> Srihari G. Nagaraju M. Murthy MM. Helv. Chim. Acta 2007, 90: 1497 <A NAME="RZ17310SS-4D">4d</A> Shaterian HR. Amirzadeh A. Khorami E. Ghashang M. Synth. Commun. 2008, 38: 2983 <A NAME="RZ17310SS-4E">4e</A> Mahdavinia GH. Bigdeli MA. Chin. Chem. Lett. 2009, 20: 383 <A NAME="RZ17310SS-5A">5a</A> Das B. Damodar K. Saritha D. Chowdhury N. Krishnaiah M. Tetrahedron Lett. 2007, 48: 7930 <A NAME="RZ17310SS-5B">5b</A> Das B. Damodar K. Shashi Kanth B. Srinivas Y. Kalavathi I. Synlett 2008, 3133 <A NAME="RZ17310SS-5C">5c</A> Das B. Damodar K. Bhunia N. J. Org. Chem. 2009, 74: 5607 <A NAME="RZ17310SS-6A">6a</A> Pearson WH. Lindbeck AC. Kampf JW. J. Am. Chem. Soc. 1933, 115: 2622 <A NAME="RZ17310SS-6B">6b</A> Mecozzi T. Petrini M. J. Org. Chem. 1999, 64: 8970 <A NAME="RZ17310SS-7A">7a</A> Petrini M. Chem. Rev. 2005, 105: 3949 <A NAME="RZ17310SS-7B">7b</A> Petrini M. Torregiani E. Synthesis 2007, 159 <A NAME="RZ17310SS-7C">7c</A> Thirupathi P. Kim SS. J. Org. Chem. 2009, 74: 7755 <A NAME="RZ17310SS-7D">7d</A> Reingruber R. Baumann T. Dabmen S. Bräse S. Adv. Synth. Catal. 2009, 351: 1019