94054-97-4Relevant academic research and scientific papers
Novel Spiro Cyclisations of N-Acyliminium Ions involving an Aromatic ?-Nucleophile
Bailey, Patrick D.,Morgan, Keith M.,Smith, David I.,Vernon, John M.
, p. 7115 - 7118 (1994)
Several spiro 2-pyrrolidin-5-ones were obtained by a two-step procedure from N-substituted succinimides, involving spiro cyclisation of N-acyliminium ion intermediates in refluxing trifluoroacetic acid; in all cases cyclisation utilised a tethered aromati
Synthesis and stereochemical determination of batzelladine C methyl ester
Butters, Michael,Davies, Christopher D.,Elliott, Mark C.,Hill-Cousins, Joseph,Kariuki, Benson M.,Ooi, Li-Ling,Wood, John L.,Wordingham, Stuart V.
experimental part, p. 5001 - 5009 (2010/02/15)
Batzelladine C (3) is a tricyclic guanidine alkaloid of unknown stereochemistry at one centre as well as unknown absolute stereochemistry. The two possible diastereoisomers of the methyl ester corresponding to this compound have been synthesised, permitti
Spiro cyclisations of N-acyliminium ions involving an aromatic π-nucleophile
Bailey, Patrick D.,Morgan, Keith M.,Smith, David I.,Vernon, John M.
, p. 3369 - 3378 (2007/10/03)
Spiro 2-pyrrolidin-5-ones were obtained from N-substituted succinimides by a two-step procedure, involving 5- or 6-endo-trig cyclisation of N-acyliminium ion intermediates with a tethered aromatic π-nucleophile.
