Literature DB >> 18044910

Chemoenzymatic synthesis of (S)-hexafluoroleucine and (S)-tetrafluoroleucine.

Hsien-Po Chiu1, Richard P Cheng.   

Abstract

We have developed a short chemoenzymatic synthesis for both (S)-5,5,5,5',5',5'-hexafluoroleucine (Hfl) and (S)-5,5,5',5'-tetrafluoroleucine (Qfl) on gram scale. Qfl was incorporated into a peptide using standard solid-phase peptide synthesis protocols to measure its helix propensity. The helix propensity for Qfl is 0.68 kcal.mol-1 more favorable compared to Hfl.

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Year:  2007        PMID: 18044910     DOI: 10.1021/ol702470j

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


  3 in total

1.  Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine.

Authors:  Holger Erdbrink; Elisabeth K Nyakatura; Susanne Huhmann; Ulla I M Gerling; Dieter Lentz; Beate Koksch; Constantin Czekelius
Journal:  Beilstein J Org Chem       Date:  2013-10-02       Impact factor: 2.883

2.  Synthesis of purines and adenines containing the hexafluoroisopropyl group.

Authors:  Viacheslav Petrov; Rebecca J Dooley; Alexander A Marchione; Brittany S Clem; William Marshall; Elizabeth L Diaz
Journal:  Beilstein J Org Chem       Date:  2020-11-11       Impact factor: 2.883

3.  Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction.

Authors:  Aline Delamare; Guillaume Naulet; Brice Kauffmann; Gilles Guichard; Guillaume Compain
Journal:  Chem Sci       Date:  2022-07-20       Impact factor: 9.969

  3 in total

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