Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/101318
Type: Artigo de periódico
Title: Stereoselective Alkylation Of N-boc-2-pyrrolidinones And N-boc-2- Piperidinones. Synthesis And Characterization Of Disubstituted Lactams
Author: Maldaner A.O.
Pilli R.A.
Abstract: Alkylation of enolates of monosubstituted N-Boc lactams 4-6 afforded trans-disubstituted lactams as the major isomer. In the pyrrolidinone series, 1,3-induction seems to be ruled by steric interactions and the diastereoselection is low for the alkylation of enolates with small substituents at C-5 (e.g., Me) and methyl iodide. The trans selectivity improves with bulkier substituents at C-2 and/or bulkier electrophiles. The formation of 3,6-trans-disubstituted piperidinones benefits from the axial orientation of the substituent at C-2 due to the A strain with the N-Boc group and excellent trans preference is observed even in the alkylation of the lithium enolate of N-Boc-6-methyl piperidinone with methyl iodide.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/S0040-4020(99)00835-2
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0033585017&partnerID=40&md5=ff8fc7d4b3340f95ba8acb45918e7899
Date Issue: 1999
Appears in Collections:Unicamp - Artigos e Outros Documentos

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