912338-18-2Relevant academic research and scientific papers
A facile preparation of an octahydropyrrolo[2,3-c]pyridine enantiomer
Shieh, Wen-Chung,Chen, Guang-Pei,Xue, Song,McKenna, Joseph,Jiang, Xinglong,Prasad, Kapa,Repic, Oljan,Straub, Christopher,Sharma, Sushil K.
, p. 711 - 715 (2012/12/29)
A facile synthesis of octahydro-pyrrolo[2,3-c]pyridine 1 using an intramolecular [3+2]-cycloaddition of an azomethine ylide as the key step and employing DW-therm heat-transfer fluid as a solvent is disclosed. Enantiomerically pure 1 was obtained either via a chromatographic separation of the diastereoisomers 12 and 13 resulting from the cycloaddition with a chiral appendage or by a classical resolution of racemate 19.
Organic compounds
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Page/Page column 77; 79, (2008/06/13)
Novel compounds that inhibit the binding of the Smac protein to Inhibitor of Apoptosis Proteins (IAPs) of the formula I
