Literature DB >> 22252910

Build/couple/pair strategy for the synthesis of stereochemically diverse macrolactams via head-to-tail cyclization.

Mark E Fitzgerald1, Carol A Mulrooney, Jeremy R Duvall, Jingqiang Wei, Byung-Chul Suh, Lakshmi B Akella, Anita Vrcic, Lisa A Marcaurelle.   

Abstract

A build/couple/pair (B/C/P) strategy was employed to generate a library of 7936 stereochemically diverse 12-membered macrolactams. All 8 stereoisomers of a common linear amine precursor were elaborated to form the corresponding 8 stereoisomers of two regioisomeric macrocyclic scaffolds via head-to-tail cyclization. Subsequently, these 16 scaffolds were further diversified via capping of two amine functionalities on SynPhase Lanterns. Reagents used for solid-phase diversification were selected using a sparse matrix design strategy with the aim of maximizing coverage of chemical space while adhering to a preset range of physicochemical properties.

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Year:  2012        PMID: 22252910      PMCID: PMC3289975          DOI: 10.1021/co200161z

Source DB:  PubMed          Journal:  ACS Comb Sci        ISSN: 2156-8944            Impact factor:   3.784


  21 in total

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5.  Fragment-based domain shuffling approach for the synthesis of pyran-based macrocycles.

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Review 6.  Macrocycles are great cycles: applications, opportunities, and challenges of synthetic macrocycles in drug discovery.

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8.  Synthesis of a stereochemically diverse library of medium-sized lactams and sultams via S(N)Ar cycloetherification.

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Journal:  ACS Comb Sci       Date:  2011-04-28       Impact factor: 3.784

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5.  Synthesis of cyclic 1,3-diols as scaffolds for spatially directed libraries.

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7.  Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosides.

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9.  Macrocycle synthesis strategy based on step-wise "adding and reacting" three components enables screening of large combinatorial libraries.

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Review 10.  Macrocyclic drugs and synthetic methodologies toward macrocycles.

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