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Pure Appl. Chem., 1963, Vol. 7, No. 2-3, pp. 269-284

The use of the Schmidt reaction in the elaboration of selected alkaloids containing a seven-membered ring

S. Uyeo

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  • Gutierrez Osvaldo, Aubé Jeffrey, Tantillo Dean J.: Mechanism of the Acid-Promoted Intramolecular Schmidt Reaction: Theoretical Assessment of the Importance of Lone Pair–Cation, Cation−π, and Steric Effects in Controlling Regioselectivity. J Org Chern 2012, 77, 640. <>
  • Crosby Ian T., Shin James K., Capuano Ben: The Application of the Schmidt Reaction and Beckmann Rearrangement to the Synthesis of Bicyclic Lactams: Some Mechanistic Considerations. Aust J Chem 2010, 63, 211. <>
  • Gracias Vijaya, Frank Kristine E., Milligan Gregory L., Aubé Jeffrey: Ring expansion by in situ tethering of hydroxy azides to ketones: The boyer reaction. Tetrahedron 1997, 53, 16241. <>
  • Mossman Craig J., Aubé Jeffrey: Intramolecular Schmidt reactions of alkyl azides with ketals and enol ethers. Tetrahedron 1996, 52, 3403. <>
  • Martínez Roberto, Avila Gustavo, Reyes Eduardo: Unusual Sulfonation of 1-(4-R-Phenyl)-2.6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindoles Under Schmidt Conditions. Synth Common 1995, 25, 1071. <>