Literature DB >> 9667836

Solid support linker strategies.

B J Backes1, J A Ellman.   

Abstract

The selection of an appropriate linker is critical to the success of any strategy for the solid-phase synthesis of small molecule libraries. While the primary function of the linker is to covalently attach the initial substrate to the support, innovative strategies have emerged recently in which linkers fulfill important auxiliary roles. These include the cleavage of compounds into solution leaving no trace of the support attachment site, cleavage via cyclization, cleavage by introduction of additional diversity into the structure, and cleavage whereby portions of the compound are sequentially released into solution.

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Year:  1997        PMID: 9667836     DOI: 10.1016/s1367-5931(97)80113-5

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  4 in total

Review 1.  Exploring privileged structures: the combinatorial synthesis of cyclic peptides.

Authors:  Douglas A Horton; Gregory T Bourne; Mark L Smythe
Journal:  J Comput Aided Mol Des       Date:  2002 May-Jun       Impact factor: 3.686

Review 2.  Exploring privileged structures: the combinatorial synthesis of cyclic peptides.

Authors:  Douglas A Horton; Gregory T Bourne; Mark L Smythe
Journal:  Mol Divers       Date:  2002       Impact factor: 2.943

3.  Temperature dependent photochemical cleavage of 2,5-dimethylphenacyl esters.

Authors:  Jaromír Literák; Stanislav Relich; Petr Kulhánek; Petr Klán
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

4.  Dialkyl Ether Formation at High-Valent Nickel.

Authors:  Franck Le Vaillant; Edward J Reijerse; Markus Leutzsch; Josep Cornella
Journal:  J Am Chem Soc       Date:  2020-11-03       Impact factor: 15.419

  4 in total

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