Literature DB >> 15469344

Caged trans-4-hydroxy-2-nonenal.

Robert G Brinson1, Paul B Jones.   

Abstract

[reaction: see text] A caged 4-hydroxy-2-nonenal (4-HNE) has been prepared and its photochemistry investigated. Upon photolysis, 1 releases 4-HNE in up to 100% yield. From these photolyses, 4-HNE could be isolated in up to 91% yield. 4-HNE is produced under either aerobic or anaerobic conditions. The caging strategy does not require prior preparation of 4-HNE and, therefore, represents a three-step synthetic route to the bioactive enal in 48% overall yield.

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Year:  2004        PMID: 15469344     DOI: 10.1021/ol048478l

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


  3 in total

Review 1.  Photoremovable protecting groups in chemistry and biology: reaction mechanisms and efficacy.

Authors:  Petr Klán; Tomáš Šolomek; Christian G Bochet; Aurélien Blanc; Richard Givens; Marina Rubina; Vladimir Popik; Alexey Kostikov; Jakob Wirz
Journal:  Chem Rev       Date:  2012-12-21       Impact factor: 60.622

2.  Temporally controlled targeting of 4-hydroxynonenal to specific proteins in living cells.

Authors:  Xinqiang Fang; Yuan Fu; Marcus J C Long; Joseph A Haegele; Eva J Ge; Saba Parvez; Yimon Aye
Journal:  J Am Chem Soc       Date:  2013-09-18       Impact factor: 15.419

3.  Time-Resolved Spectroscopic Study on the Photoredox Reaction of 2-(p-Hydroxymethyl)phenylAnthraquinone.

Authors:  Qingqing Song; Xiting Zhang; Jiani Ma; Yan Guo; David Lee Phillips
Journal:  Sci Rep       Date:  2017-08-22       Impact factor: 4.379

  3 in total

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