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

http://dx.doi.org/10.1351/pac196307020269

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

S. Uyeo

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  • Nami Shahab A. A., Khan Suraiya, Alam Mahboob, Mushfiq M., Lee Dong-Ung, Park Soonheum: Synthesis, Spectral Characterization, and In Vitro Cytotoxicity of N-2′-Hydroxyethyl-Substituted Azacholestanes Prepared from 6-Oxocholestanes by Modified Schmidt Reaction. Journal of Spectroscopy 2013, 2013, 1. <http://dx.doi.org/10.1155/2013/128149>
  • 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. <http://dx.doi.org/10.1021/jo202338m>
  • 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. <http://dx.doi.org/10.1071/CH09402>
  • 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. <http://dx.doi.org/10.1016/S0040-4020(97)01012-0>
  • Mossman Craig J., Aubé Jeffrey: Intramolecular Schmidt reactions of alkyl azides with ketals and enol ethers. Tetrahedron 1996, 52, 3403. <http://dx.doi.org/10.1016/0040-4020(96)00037-3>
  • 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. <http://dx.doi.org/10.1080/00397919508012669>