Literature DB >> 30906077

Stereocontrolled synthesis of four isomeric linoleate triols of relevance to skin barrier formation and function.

Robert W Davis1, Alexander Allweil1, Jianhua Tian1, Alan R Brash2, Gary A Sulikowski1,2.   

Abstract

Linoleate triol esters are intermediates along the pathway of formation of the mammalian skin permeability barrier. In connection with the study of their involvement in barrier formation we required access to isomerically pure and defined samples of four linoleate triol esters. A common synthetic strategy was developed starting from isomeric alkynols derived from d-tartaric acid and 2-deoxy-d-ribose.

Entities:  

Keywords:  Fatty acids; Stereochemistry; Synthesis strategy; Total synthesis

Year:  2018        PMID: 30906077      PMCID: PMC6424341          DOI: 10.1016/j.tetlet.2018.11.033

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


  2 in total

1.  Stable analogs of 13‑hydroxy-9,10-trans-epoxy-(11E)-octadecenoate (13,9-HEL), an oxidized derivative of linoleic acid implicated in the epidermal skin barrier.

Authors:  Gregory S Keyes; Kristen Maiden; Christopher E Ramsden
Journal:  Prostaglandins Leukot Essent Fatty Acids       Date:  2021-10-24       Impact factor: 4.006

2.  SDR9C7 catalyzes critical dehydrogenation of acylceramides for skin barrier formation.

Authors:  Takuya Takeichi; Tetsuya Hirabayashi; Yuki Miyasaka; Akane Kawamoto; Yusuke Okuno; Shijima Taguchi; Kana Tanahashi; Chiaki Murase; Hiroyuki Takama; Kosei Tanaka; William E Boeglin; M Wade Calcutt; Daisuke Watanabe; Michihiro Kono; Yoshinao Muro; Junko Ishikawa; Tamio Ohno; Alan R Brash; Masashi Akiyama
Journal:  J Clin Invest       Date:  2020-02-03       Impact factor: 14.808

  2 in total

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