Nucleophilic synthesis of enantiopure 2-(tributylstannyl) pyrrolidines and piperidines
…, G Barolli, S Madan, M Saverin, S O'Connor
Index: Gawley, Robert E.; Barolli, Graciela; Madan, Sachin; Saverin, Michele; O'Connor, Sean Tetrahedron Letters, 2004 , vol. 45, # 8 p. 1759 - 1761
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Citation Number: 17
Abstract
trans-Cumylcyclohexanol (TCC) is used as a chiral auxiliary for the stereoselective addition of tributyltinlithium to N-acylpyrrolidinium/piperidinium ion with 70–80% diastereoselectivity at 0° C. After removal of the minor diastereomer by radial chromatography, enantiopure N- methyl-2-(tributylstannyl) pyrrolidine and piperidine were produced by reductive removal of the auxiliary.
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