Literature DB >> 21082790

Synthesis of β-keto esters in-flow and rapid access to substituted pyrimidines.

Hannah E Bartrum1, David C Blakemore, Christopher J Moody, Christopher J Hayes.   

Abstract

We have developed an in-flow process for the synthesis of β-keto esters via the BF(3)·OEt(2)-catalyzed formal C-H insertion of ethyl diazoacetate into aldehydes. The β-keto esters were then condensed with a range of amidines to give a variety of 2,6-substituted pyrimidin-4-ols.

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Year:  2010        PMID: 21082790     DOI: 10.1021/jo101783m

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Ethyl diazoacetate synthesis in flow.

Authors:  Mariëlle M E Delville; Jan C M van Hest; Floris P J T Rutjes
Journal:  Beilstein J Org Chem       Date:  2013-09-05       Impact factor: 2.883

  1 in total

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