Regiospecific synthesis and biological evaluation of spirooxindolopyrrolizidines via [3+2] cycloaddition of azomethine ylide
- 31 December 2010
- journal article
- research article
- Published by Elsevier BV in European Journal of Medicinal Chemistry
- Vol. 45 (12), 6120-6126
- https://doi.org/10.1016/j.ejmech.2010.09.051
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- A highly regioselective synthesis of 1-n-methyl-spiro-[2,3′“]-oxindole-spiro-[3,2”]indane-1“, 3”-dione-4-arylpyrrolidines through 1,3-dipolar cycloaddition protocolJournal of Heterocyclic Chemistry, 2006
- Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole AlkaloidsEuropean Journal of Organic Chemistry, 2003
- Total Synthesis of Spirotryprostatin A, Leading to the Discovery of Some Biologically Promising AnaloguesJournal of the American Chemical Society, 1999
- Ein einfacher Zugang zu den tetracyclischen Vorläufern der Hetero- und Secoyohimbane, Strychnos- und OxindolalkaloideEuropean Journal of Organic Chemistry, 1994
- On the Synthesis of the Oxindole Alkaloid: (±)-HorsfilineHETEROCYCLES, 1994
- Horsfiline, an oxindole alkaloid from Horsfieldia superbaThe Journal of Organic Chemistry, 1991
- Iminium ion route to azomethine yields from primary and secondary aminesJournal of the Chemical Society, Chemical Communications, 1986
- Decarboxylative transamination. A new route to spirocyclic and bridgehead-nitrogen compounds. Relevance to α-amino acid decarboxylasesJournal of the Chemical Society, Chemical Communications, 1984
- Decarboxylative transamination. Mechanism and applications to the synthesis of heterocyclic compoundsJournal of the Chemical Society, Chemical Communications, 1984
- The Molecular and Crystal Structure of an Oxindole Alkaloid (6-Hydroxy-2′-(2-methylpropyl)-3,3′-spirotetrahydropyrrolidino-oxindole)Canadian Journal of Chemistry, 1972