Literature DB >> 22136351

Enantio- and diastereoselective organocatalytic α-alkylation of aldehydes with 3-substituted 2-(bromomethyl)acrylates.

Jacqueline Jiménez1, Aitor Landa, Aitziber Lizarraga, Miguel Maestro, Antonia Mielgo, Mikel Oiarbide, Irene Velilla, Claudio Palomo.   

Abstract

The catalytic direct α-alkylation of aldehydes with 2-(bromomethyl)acrylates has been accomplished, giving rise to α-branched and functionalized aldehydes of high diastereo- and enantiopurity. The influence of the nature of the ester group of the acrylates in reaction stereoselectivity and especially in reactivity is investigated. Optimum conditions implicate the use of phenyl acrylates in conjunction with organocatalyst 8. Application of thus obtained adducts in synthesis is illustrated with a concise stereocontrolled preparation of trisubstituted cyclopentenes.

Entities:  

Year:  2011        PMID: 22136351     DOI: 10.1021/jo202073n

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


  2 in total

1.  Experimental and Computational Studies Unraveling the Peculiarity of Enolizable Oxoesters in the Organocatalyzed Mannich-Type Addition to Cyclic N-Acyl Iminium Ions.

Authors:  Andrea Menichetti; Sebastiano Di Pietro; Valeria Di Bussolo; Lucilla Favero; Mauro Pineschi
Journal:  Molecules       Date:  2020-04-20       Impact factor: 4.411

2.  Asymmetric intramolecular α-cyclopropanation of aldehydes using a donor/acceptor carbene mimetic.

Authors:  Chaosheng Luo; Zhen Wang; Yong Huang
Journal:  Nat Commun       Date:  2015-12-08       Impact factor: 14.919

  2 in total

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