The Unility of the Pummerer Rearrangement Intermediates in the Presence of Lewis Acids—A Short and Practical Synthesis of 4-(2-Di-n-Propylaminoethyl)-7-methoxyindole

Christos G. Gourdoupis University of Patras, School of Health Sciences, Department of Pharmacy, Rion, Patras, 261 10, Hellas

Ioannis K. Stamos The National Hellenic Research Foundation, Institute of Organic and Pharmaceutical Chemistry and the Center for Molecular Analysis, 48 V. Konstantinou Ave., Athens, 116 35, Hellas

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BarryP. Clark & JohnR. Harris. (1997) Syntheses of 7-Carboxyindolylglycines Utilising Glycine Cation Equivalents. Synthetic Communications 27:24, pages 4223-4234.
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Christopher J. Trabbic, Sage M. George, Evan M. Alexander, Shengnan Du, Jennifer M. Offenbacher, Emily J. Crissman, Jean H. Overmeyer, William A. Maltese & Paul W. Erhardt. (2016) Synthesis and biological evaluation of isomeric methoxy substitutions on anti-cancer indolyl-pyridinyl-propenones: Effects on potency and mode of activity. European Journal of Medicinal Chemistry 122, pages 79-91.
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Ioannis K. Stamos & Heleni K. Kotzamani. (2009) The potential utility of homoacylation through the pummerer rearrangement‐intermediates. A direct approach to the 1‐benzene‐sulfonyl‐4‐keto‐8‐methoxy‐1,2,2a,3,4,5‐hexahydrobenz‐[ cd ]indole via intra‐homoacylation . Journal of Heterocyclic Chemistry 32:3, pages 947-951.
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C. G. GOURDOUPIS & I. K. STAMOS. (2010) ChemInform Abstract: The Utility of the Pummerer Rearrangement Intermediates in the Presence of Lewis Acids. A Short and Practical Synthesis of 4‐(2‐Di‐n‐ propylaminoethyl)‐7‐methoxyindole (V).. ChemInform 25:43.
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The Unility of the Pummerer Rearrangement Intermediates in the Presence of Lewis Acids—A Short and Practical Synthesis of 4-(2-Di-n-Propylaminoethyl)-7-methoxyindole

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The Unility of the Pummerer Rearrangement Intermediates in the Presence of Lewis Acids—A Short and Practical Synthesis of 4-(2-Di-n-Propylaminoethyl)-7-methoxyindole

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