Literature DB >> 11300885

Mixed organofluorine-organosilicon chemistry. 13. One-pot synthesis of difluoroaldols from acylsilanes and trifluoromethyltrimethylsilane. application to the synthesis of a difluoro analogue of egomaketone.

O Lefebvre1, T Brigaud, C Portella.   

Abstract

Difluoroaldol compounds 3 were synthesized in a one-pot procedure involving an acylsilane 1, trifluoromethyltrimethylsilane (TFMTMS), and an aldehyde. The key intermediate of this reaction is a difluoroenoxysilane 2. Ytterbium triflate proved to be a very efficient catalyst for promoting the aldol type reaction under very mild conditions. The potential of this reaction for the convergent synthesis of difluorinated compounds was illustrated by the synthesis of difluoroegomaketone 7d through dehydration of the corresponding aldol compound 3d.

Entities:  

Year:  2001        PMID: 11300885     DOI: 10.1021/jo001549j

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


  4 in total

1.  Divergent stereocontrol of acid catalyzed intramolecular aldol reactions of 2,3,7-triketoesters: synthesis of highly functionalized cyclopentanones.

Authors:  Phong Truong; Charles S Shanahan; Michael P Doyle
Journal:  Org Lett       Date:  2012-06-28       Impact factor: 6.005

2.  Asymmetric catalytic Mannich-type reaction of hydrazones with difluoroenoxysilanes using imidazoline-anchored phosphine ligand-zinc(II) complexes.

Authors:  Zhiliang Yuan; Liangyong Mei; Yin Wei; Min Shi; Padmanabha V Kattamuri; Patrick McDowell; Guigen Li
Journal:  Org Biomol Chem       Date:  2012-02-15       Impact factor: 3.876

3.  Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate.

Authors:  Atsushi Tarui; Mayuna Oduti; Susumu Shinya; Kazuyuki Sato; Masaaki Omote
Journal:  RSC Adv       Date:  2018-06-05       Impact factor: 3.361

4.  Syn-selective silicon Mukaiyama-type aldol reactions of (pentafluoro-λ6-sulfanyl)acetic acid esters with aldehydes.

Authors:  Anna-Lena Dreier; Andrej V Matsnev; Joseph S Thrasher; Günter Haufe
Journal:  Beilstein J Org Chem       Date:  2018-02-08       Impact factor: 2.883

  4 in total

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