Literature DB >> 21858368

Base-free two-step synthesis of 1,3-diketones and β-ketoesters from α-diazocarbonyl compounds, trialkylboranes, and aromatic aldehydes.

Miguel A Sanchez-Carmona1, David A Contreras-Cruz, Luis D Miranda.   

Abstract

We describe a convergent, base-free two-step synthesis of 1,3-diketones and β-ketoesters from α-diazocarbonyl compounds, trialkylboranes, and aromatic aldehydes in a three-component process. The synthetic potential of this protocol was underscored by the synthesis of several symmetrical 1,3,5-triaryl-4-alkyl and 1,3,4,5-tetraryl substituted pyrazoles in a three-step sequence.

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Year:  2011        PMID: 21858368     DOI: 10.1039/c1ob05150d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Diastereoselective three-component synthesis of β-amino carbonyl compounds using diazo compounds, boranes, and acyl imines under catalyst-free conditions.

Authors:  Yi Luan; Jie Yu; Xiaowei Zhang; Scott E Schaus; Ge Wang
Journal:  J Org Chem       Date:  2014-05-07       Impact factor: 4.354

  1 in total

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