36944-99-7Relevant academic research and scientific papers
Ruthenium-NHC-Catalyzed asymmetric hydrogenation of indolizines: Access to indolizidine alkaloids
Ortega, Nuria,Tang, Dan-Tam D.,Urban, Slawomir,Zhao, Dongbing,Glorius, Frank
supporting information, p. 9500 - 9503 (2013/09/23)
Crossing N-bridges! A ruthenium/N-heterocyclic carbene (NHC) complex serves as the catalyst for the high-yielding and completely regioselective and asymmetric hydrogenation of substituted indolizines and 1,2,3-triazolo-[1,5-a] pyridines. This method shoul
Synthesis of functionalized indolizines via copper-catalyzed annulation of 2-alkylazaarenes with α,β-unsaturated carboxylic acids
Yang, Yuzhu,Xie, Chunsong,Xie, Yongju,Zhang, Yuhong
supporting information; experimental part, p. 957 - 959 (2012/04/04)
A novel copper-catalyzed annulation of 2-alkylazaarenes with α,β-unsaturated carboxylic acids has been accomplished. This reaction featuring C-H olefination and decarboxylative amination processes provides a concise access to C-2 arylated indolizines from simple and readily available starting materials.
Metallation of 2-phenylindolizine
Renard, Michel
, p. 4433 - 4434 (2007/10/02)
Regioselective metallation of 2-phenylindolizine at C(5) and subsequent reaction with an electrophile has afforded the corresponding C(5) functionalised indolizine in high yields.
Heterocyclic Compounds with Bridgehead Nitrogen atoms: Part 9. Synthesis in the Pyrroloquinolizine (Cyclazine) Series starting from Indolizines
Dick, James W.,Gibson, William K.,Leaver, Derek,Roff, John E.
, p. 3150 - 3157 (2007/10/02)
Pyrroloquinolizines may be obtained from various 3-substituted derivatives of 5-methyl-2-phenyl- and 2,5-dimethyl-indolizine by base-catalysed condensation of the 5-methyl group with a carbonyl group in the β-position of the 3-substituent.The 1,
