Literature DB >> 12556184

Asymmetric halo aldol reaction (AHA).

Guigen Li1, Xin Xu, Dianjun Chen, Cody Timmons, Michael D Carducci, Allan D Headley.   

Abstract

[reaction: see text] The asymmetric halo aldol reaction (AHA) using Evans oxazolidinones as chiral auxiliaries has been established for tandem I-C/C-C bond formations. The new asymmetric reaction provides a practical approach to a variety of halo aldols of a non-Evans type that cannot be easily synthesized by other methods. Excellent diastereoselectivity (>95%) and yields (80-93%) have been obtained for eight examples.

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Year:  2003        PMID: 12556184     DOI: 10.1021/ol027344+

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Efficient assembly of 2,5,6-substituted pyrimidines via MgI(2)-mediated Morita-Baylis-Hillman reaction.

Authors:  Vasudha Sharma; Mark L McLaughlin
Journal:  J Comb Chem       Date:  2010-05-10

2.  Allenoate Prenucleophiles: A Triply Diastereoselective Approach to β-Hydroxy Esters Containing All-Carbon α-Quaternary Centers.

Authors:  Samantha L Maki; Pradip Maity; Shannon Dougherty; Jennifer Johns; Salvatore D Lepore
Journal:  Org Lett       Date:  2019-09-16       Impact factor: 6.072

  2 in total

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