Total syntheses of yohimbe alkaloids, with stereoselection for the normal, allo, and 3-epiallo series, based on annelations of 4-methoxy-1, 2-dihydropyridones
ME Kuehne, RS Muth
Index: Kuehne, Martin E.; Muth, Randy S. Journal of Organic Chemistry, 1991 , vol. 56, # 8 p. 2701 - 2712
Full Text: HTML
Citation Number: 61
Abstract
Background Starting with the synthesis of yohimbone by Swan in 1950,'synthetic studies directed at the Yohimbe alkaloids have provided a variety of approaches that, apart from their specific goals, advanced organic chemistry through the development of important synthetic methodologies. While a complete review of those syntheses is beyond the scope of this paper (and already available): we summarize here, for comparison, only the most ...
Related Articles:
Formylation of amines through catalyst-and solvent-free transamidation reaction
[Lebleu, Thomas; Kotsuki, Hiyoshizo; Maddaluno, Jacques; Legros, Julien Tetrahedron Letters, 2014 , vol. 55, # 2 p. 362 - 364]
Novel chemistry of β-carbolines. Expedient synthesis of polycyclic scaffolds
[Gonzalez-Gomez, Alvaro; Dominguez, Gema; Perez-Castells, Javier Tetrahedron, 2009 , vol. 65, # 17 p. 3378 - 3391]
Structure and Reactivity of Indolylmethylium Ions: Scope and Limitations in Synthetic Applications
[Mueller, Johann; Pindur, Ulf Archiv der Pharmazie (Weinheim, Germany), 1984 , vol. 317, # 6 p. 555 - 561]
Synthesis of 2-(3′-Indolyl) tetrahydrofurans by Oxidative Cycloetherification
[Yoshioka, Tadao; Mohri, Kunihiko; Oikawa, Yuji; Yonemitsu, Osamu Journal of Chemical Research, Miniprint, 1981 , # 7 p. 2252 - 2281]