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- An efficient Ugi-3CR/aza Diels–Alder/Pomeranz–Fritsch protocol towards novel aza-analogues of (±)-nuevamine, (±)-lennoxamine and magallanesine: a diversity oriented synthesis approach. Óscar Vázquez-Vera, Jorge S. Sánchez-Badillo, Alejandro Islas-Jácome, Manuel A. Rentería-Gómez, Shrikant G. Pharande, Carlos J. Cortes-García, Mónica A. Rincón-Guevara, Ilich A. Ibarra, Rocío Gámez-Montaño, Eduardo González-Zamora
, Org. Biomol. Chem.
, 2017
, 15
, 2363
- Vinyl azides in heterocyclic synthesis. Part 10. Synthesis of the isoindolobenzazepine alkaloid lennoxamine. Christopher J. Moody, Graham J. Warrellow
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 2929
- An efficient method for the synthesis of enol ethers and enecarbamates. Total syntheses of isoindolobenzazepine alkaloids, lennoxamine and chilenine. Haruhiko Fuwa, Makoto Sasaki
, Org. Biomol. Chem.
, 2007
, 5
, 1849
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Sulfur-controlled 5-exo selective aryl radical
cyclisation of N-vinylic 2-bromobenzamides: synthesis
of lennoxamine and chilenine
. Hiroyuki Ishibashi, Hirotaka Kawanami, Masazumi Ikeda
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 817
- A simple total synthesis of the isoindolobenzazepine alkaloids lennoxamine and chilenamine. Elio Napolitano, Guido Spinelli, Rita Fiaschi, Antonio Marsili
, J. Chem. Soc., Perkin Trans. 1
, 1986
, 785
- The Ugi three-component reaction and its variants. Julio César Flores-Reyes, Alejandro Islas-Jácome, Eduardo González-Zamora
, Org. Chem. Front.
, 2021
, 8
, 5460
- Rapid access to tetracyclic ring system of lennoxamine type natural product by combined use of a novel three-component reaction and Pummerer cyclization. Rocio Gámez Montaño, Jieping Zhu
, Chem. Commun.
, 2002
, 2448
- β-Phenylethylamines and the isoquinoline alkaloids. Kenneth W. Bentley
, Nat. Prod. Rep.
, 2005
, 22
, 249
- β-Phenylethylamines and the isoquinoline
alkaloids. Kenneth W. Bentley
, Nat. Prod. Rep.
, 2000
, 17
, 247
- Enamides: valuable organic substrates. David R. Carbery
, Org. Biomol. Chem.
, 2008
, 6
, 3455