111479-54-0Relevant academic research and scientific papers
Bicyclic σ receptor ligands by stereoselective Dieckmann analogous cyclization of piperazinebutyrate
Sunnam, Sunil Kumar,Schepmann, Dirk,Wibbeling, Birgit,Wuensch, Bernhard
experimental part, p. 3715 - 3722 (2010/09/06)
Starting from racemic 2-aminoadipic acid (6) the piperazinedione 10 with a butyrate side chain was synthesized in four reaction steps. The four-carbon bridge was established upon deprotonation of 10 with LHMDS and subsequent trapping of the lithium alcoholate with Me3SiCl to give diastereoselectively the mixed methyl silyl ketal 12 in 94% yield. The relative configuration of the new center of chirality was determined by X-ray crystal structure analysis of 12. The high diastereoselectivity during the conversion of the butyrate 10 into the mixed methyl silyl ketal 12 supports the formation of the lithium alcoholate 11 as central intermediate. Stereoselective reduction of the ketone 13 with LiBH4 led to the alcohol 14, which was benzylated and reduced to provide the final bicyclic products 16 and 17. Whereas the alcohol 16 shows only moderate affinity to both σ receptor subtypes, the benzyl ether 17 represents a potent and selective σ1 receptor ligand (Ki = 47 nM). Comparison of the σ receptor affinities of 16 and 17 with the smaller homologues 5a and 5c clearly indicates that the size of the bridge and the O-substituent determines subtype selectivity.
ALKYLATION OF SHIFF BASE ANIONS WITH ω-HALOGENO ESTERS: A LACTAM SYNTHESIS.
Mkhairi, A,Hamelin, J.
, p. 4435 - 4436 (2007/10/02)
Imine anions of α-aminoesters, obtained from NaH/DMSO are alkylated with ω-halogenoesters.Thermolysis of the alkylated compounds lead to functionnalized lactams.
