Highly Stereoselective and Scalable Synthesis of trans-Fused Octahydrocyclohepta[b]pyrrol-4(1H)-ones via the Aza-Cope-Mannich Rearrangement in Racemic and Enantiopure Forms Article

Belov, Dmitry S, Lukyanenko, Evgeny R, Kurkin, Alexander V et al. (2012). Highly Stereoselective and Scalable Synthesis of trans-Fused Octahydrocyclohepta[b]pyrrol-4(1H)-ones via the Aza-Cope-Mannich Rearrangement in Racemic and Enantiopure Forms . JOURNAL OF ORGANIC CHEMISTRY, 77(22), 10125-10134. 10.1021/jo301762a

cited authors

  • Belov, Dmitry S; Lukyanenko, Evgeny R; Kurkin, Alexander V; Yurovskaya, Marina A

sustainable development goals

authors

publication date

  • November 16, 2012

webpage

published in

keywords

  • 5,11-METHANOMORPHANTHRIDINE TYPE
  • AMARYLLIDACEAE ALKALOIDS
  • ASPIDOSPERMA ALKALOIDS
  • CARBON BOND FORMATION
  • COMBINATORIAL LIBRARIES
  • CYCLIZATION REACTIONS
  • Chemistry
  • Chemistry, Organic
  • ENANTIOSELECTIVE TOTAL-SYNTHESIS
  • GRIGNARD-REAGENTS
  • NUCLEOPHILIC-ADDITION
  • Physical Sciences
  • STEREOCONTROLLED TOTAL-SYNTHESIS
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • AMER CHEMICAL SOC

start page

  • 10125

end page

  • 10134

volume

  • 77

issue

  • 22