Literature DB >> 16292871

Lewis base catalyzed enantioselective aldol addition of acetaldehyde-derived silyl enol ether to aldehydes.

Scott E Denmark1, Tommy Bui.   

Abstract

[reaction: see text] Chiral phosphoramide catalyzed-enantioselective aldol addition of an acetaldehyde-derived trialkylsilyl enol ether to aromatic aldehydes provides protected aldol products in good yields with good to excellent enantioselectivities. Preliminary studies show that the aldolization intermediate (a chlorohydrin adduct) can be trapped with tert-butyl isocyanide to form an alpha-hydroxy lactone with good selectivity in a single-pot operation.

Entities:  

Year:  2005        PMID: 16292871     DOI: 10.1021/jo0517500

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


  3 in total

1.  Rapid and stereochemically flexible synthesis of polypropionates: super-silyl-governed aldol cascades.

Authors:  Patrick B Brady; Hisashi Yamamoto
Journal:  Angew Chem Int Ed Engl       Date:  2012-01-17       Impact factor: 15.336

2.  A triple-aldol cascade reaction for the rapid assembly of polyketides.

Authors:  Brian J Albert; Hisashi Yamamoto
Journal:  Angew Chem Int Ed Engl       Date:  2010-04-01       Impact factor: 15.336

3.  An Efficient Boric Acid Mediated Preparation of α-Hydroxyamides.

Authors:  J Sravan Kumar; Subash C Jonnalagadda; Venkatram R Mereddy
Journal:  Tetrahedron Lett       Date:  2010-02-03       Impact factor: 2.415

  3 in total

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