Literature DB >> 21846123

Use of catalytic fluoride under neutral conditions for cleaving silicon-oxygen bonds.

Anthony M DiLauro1, Wanji Seo, Scott T Phillips.   

Abstract

This Article describes the development of conditions for cleaving silicon-oxygen bonds using catalytic quantities of fluoride at neutral pH in mixed organic-aqueous solutions that contain buffer. A variety of silicon protecting groups can be removed under these conditions, which show tolerance for acid- and base-sensitive groups. A modified procedure also is presented using catalytic fluoride in anhydrous dimethyl sulfoxide-methanol, which generates primarily volatile silicon byproducts.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21846123     DOI: 10.1021/jo200848j

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


  3 in total

1.  Analysis and Identification of 2'-Deoxyadenosine-Derived Adducts in Lung and Liver DNA of F-344 Rats Treated with the Tobacco-Specific Carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone and Enantiomers of its Metabolite 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol.

Authors:  Erik S Carlson; Pramod Upadhyaya; Peter W Villalta; Bin Ma; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2018-04-19       Impact factor: 3.739

2.  Catalytic Enantioselective Peroxidation of α,β-Unsaturated Aldehydes for the Asymmetric Synthesis of Biologically Important Chiral Endoperoxides.

Authors:  Lin Hu; Xiaojie Lu; Li Deng
Journal:  J Am Chem Soc       Date:  2015-06-29       Impact factor: 15.419

3.  Overcoming synthetic challenges in targeting coenzyme A biosynthesis with the antimicrobial natural product CJ-15,801.

Authors:  Riyad Domingo; Renier van der Westhuyzen; Anton R Hamann; Konrad J Mostert; Leanne Barnard; Tanya Paquet; Erick T Tjhin; Kevin J Saliba; Willem A L van Otterlo; Erick Strauss
Journal:  Medchemcomm       Date:  2019-10-17       Impact factor: 3.597

  3 in total

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