Literature DB >> 29056780

Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged chiral oxazolidinones.

Serhan Turkyilmaz1,2, Craig S Wilcox1.   

Abstract

Sorting tags are oligomeric structures that can be used as protecting groups or chiral auxiliaries enabling solution-phase mixture syntheses of multiple tagged compounds in one pot and allowing for facile and predictable chromatographic separation of products at the end of synthetic sequences. Perfluorinated hydrocarbon and oligomeric ethylene glycol (OEG) derivatives are known classes of sorting tags. Herein we describe the preparation of OEGylated chiral oxazolidinones and their use in asymmetric solution-phase mixture aldol reactions. Through the use of such oxazolidinones based on tyrosine four different individually tagged aldol adducts were obtained as a mixture, chromatographically demixed, detagged, and it was shown that these processes gave the desired aldol products in good yield and enantioselectivity.

Entities:  

Keywords:  Evans Aldol Reaction; Oligomeric Ethylene Glycol; Oxazolidinone; Solution-Phase Mixture Synthesis; Sorting Tag

Year:  2017        PMID: 29056780      PMCID: PMC5646709          DOI: 10.1016/j.tetlet.2017.04.026

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  25 in total

1.  Precipitons-Functional Protecting Groups to Facilitate Product Separation: Applications in Isoxazoline Synthesis.

Authors:  Todd Bosanac; Jaemoon Yang; Craig S. Wilcox
Journal:  Angew Chem Int Ed Engl       Date:  2001-05-18       Impact factor: 15.336

2.  Quasiracemic synthesis: concepts and implementation with a fluorous tagging strategy to make both enantiomers of pyridovericin and mappicine.

Authors:  Qisheng Zhang; Alexey Rivkin; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2002-05-22       Impact factor: 15.419

3.  Precipiton reagents: precipiton phosphines for solution-phase reductions.

Authors:  Todd Bosanac; Craig S Wilcox
Journal:  Org Lett       Date:  2004-07-08       Impact factor: 6.005

4.  Solution-phase mixture synthesis with double-separation tagging: double demixing of a single mixture provides a stereoisomer library of 16 individual murisolins.

Authors:  Craig S Wilcox; Venugopal Gudipati; Hejun Lu; Serhan Turkyilmaz; Dennis P Curran
Journal:  Angew Chem Int Ed Engl       Date:  2005-10-28       Impact factor: 15.336

5.  Solution-phase parallel synthesis with oligoethylene glycol sorting tags. Preparation of all four stereoisomers of the hydroxybutenolide fragment of murisolin and related acetogenins.

Authors:  Venugopal Gudipati; Dennis P Curran; Craig S Wilcox
Journal:  J Org Chem       Date:  2006-04-28       Impact factor: 4.354

6.  Fluorous mixture synthesis: a fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds.

Authors:  Z Luo; Q Zhang; Y Oderaotoshi; D P Curran
Journal:  Science       Date:  2001-03-02       Impact factor: 47.728

7.  Structure assignment of lagunapyrone B by fluorous mixture synthesis of four candidate stereoisomers.

Authors:  Fanglong Yang; Jeffery J Newsome; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2006-11-01       Impact factor: 15.419

8.  Multistep phase-switch synthesis by using liquid-liquid partitioning of boronic acids: productive tags with an expanded repertoire of compatible reactions.

Authors:  Sam Mothana; Jean-Marie Grassot; Dennis G Hall
Journal:  Angew Chem Int Ed Engl       Date:  2010-02-09       Impact factor: 15.336

9.  Bare-minimum fluorous mixture synthesis of a stereoisomer library of 4,8,12-trimethylnonadecanols and predictions of NMR spectra of saturated oligoisoprenoid stereoisomers.

Authors:  Edmund A-H Yeh; Eveline Kumli; Krishnan Damodaran; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2013-01-18       Impact factor: 15.419

10.  Binary fluorous tagging enables the synthesis and separation of a 16-stereoisomer library of macrosphelides.

Authors:  Dennis P Curran; Mantosh K Sinha; Kai Zhang; Jesse J Sabatini; Dae-Hyun Cho
Journal:  Nat Chem       Date:  2012-01-10       Impact factor: 24.427

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