| Literature DB >> 10930264 |
R K Dieter1, H Yu.
Abstract
alpha-Aminoalkylcuprates prepared from CuX.2LiCl (X = Cl, CN) and 1 equiv of an alpha-lithiocarbamate undergo conjugate addition reactions to alpha,beta-alkynyl ketones in moderate to good yields, affording E:Z mixtures of alpha,beta-enones. Treatment of the conjugate adducts with PhOH/TMSCl in CH(2)Cl(2) effected carbamate deprotection and cyclization to afford a flexible two-step synthesis of substituted pyrroles.Entities:
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Year: 2000 PMID: 10930264 DOI: 10.1021/ol006050q
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005