Total synthesis and structural validation of cyclodepsipeptides solonamide A and B

[1]  L. Gram,et al.  Solonamide B Inhibits Quorum Sensing and Reduces Staphylococcus aureus Mediated Killing of Human Neutrophils , 2014, PloS one.

[2]  Kieron M. G. O'Connell,et al.  Combating multidrug-resistant bacteria: current strategies for the discovery of novel antibacterials. , 2013, Angewandte Chemie.

[3]  C. Olsen,et al.  Total synthesis and full histone deacetylase inhibitory profiling of Azumamides A-E as well as β²- epi-Azumamide E and β³-epi-Azumamide E. , 2013, Journal of medicinal chemistry.

[4]  Vipin Chandra Kalia,et al.  Quorum sensing inhibitors: an overview. , 2013, Biotechnology advances.

[5]  A. Venkatesham,et al.  Stereoselective total synthesis of stagonolide-C , 2012 .

[6]  M. Ghadiri,et al.  Macrocyclic peptoid-Peptide hybrids as inhibitors of class I histone deacetylases. , 2012, ACS medicinal chemistry letters.

[7]  M. Ghadiri,et al.  Discovery of HDAC Inhibitors That Lack an Active Site Zn(2+)-Binding Functional Group. , 2012, ACS medicinal chemistry letters.

[8]  A. Venkatesham,et al.  Stereoselective synthesis towards verbalactone and (+)-(3R,5R)-3-hydroxy-5-decanolide , 2012 .

[9]  L. Gram,et al.  Inhibition of Virulence Gene Expression in Staphylococcus aureus by Novel Depsipeptides from a Marine Photobacterium , 2011, Marine drugs.

[10]  J. M. Takacs,et al.  Catalytic asymmetric hydroboration of β,γ-unsaturated Weinreb amides: striking influence of the borane. , 2011, Chemical communications.

[11]  D. Sturdevant,et al.  Role of the Accessory Gene Regulator agr in Community-Associated Methicillin-Resistant Staphylococcus aureus Pathogenesis , 2011, Infection and Immunity.

[12]  M. Otto Basis of virulence in community-associated methicillin-resistant Staphylococcus aureus. , 2010, Annual review of microbiology.

[13]  V. Sperandio,et al.  Anti-virulence strategies to combat bacteria-mediated disease , 2010, Nature Reviews Drug Discovery.

[14]  M. Ghadiri,et al.  Discovery of potent and selective histone deacetylase inhibitors via focused combinatorial libraries of cyclic alpha3beta-tetrapeptides. , 2009, Journal of medicinal chemistry.

[15]  H. Ingmer,et al.  Method for Screening Compounds That Influence Virulence Gene Expression in Staphylococcus aureus , 2009, Antimicrobial Agents and Chemotherapy.

[16]  F. DeLeo,et al.  Reemergence of antibiotic-resistant Staphylococcus aureus in the genomics era. , 2009, The Journal of clinical investigation.

[17]  Henry F. Chambers,et al.  Waves of resistance: Staphylococcus aureus in the antibiotic era , 2009, Nature Reviews Microbiology.

[18]  John M. Beierle,et al.  Design, synthesis, biological evaluation, and structural characterization of potent histone deacetylase inhibitors based on cyclic alpha/beta-tetrapeptide architectures. , 2009, Journal of the American Chemical Society.

[19]  A. Ganesan,et al.  Macrolactamization versus macrolactonization: total synthesis of FK228, the depsipeptide histone deacetylase inhibitor. , 2008, The Journal of organic chemistry.

[20]  P. Skaanderup,et al.  Synthesis of the macrocyclic core of (-)-pladienolide B. , 2008, Organic letters.

[21]  J. Yadav,et al.  A Concise Stereoselective Total Synthesis of Herbarumin III , 2008 .

[22]  A. Clatworthy,et al.  Targeting virulence: a new paradigm for antimicrobial therapy , 2007, Nature Chemical Biology.

[23]  T. Muir,et al.  Molecular Mechanisms of agr Quorum Sensing in Virulent Staphylococci , 2007, Chembiochem : a European journal of chemical biology.

[24]  A. Ganesan,et al.  Total synthesis of azumamide A and azumamide E, evaluation as histone deacetylase inhibitors, and design of a more potent analogue. , 2007, Organic letters.

[25]  Hiroshi Tomoda,et al.  Synthesis and biological evaluation of a beauveriolide analogue library. , 2006, Journal of combinatorial chemistry.

[26]  J. Schmid,et al.  A Broad Diversity of Volatile Carboxylic Acids, Released by a Bacterial Aminoacylase from Axilla Secretions, as Candidate Molecules for the Determination of Human‐Body Odor Type , 2006, Chemistry & biodiversity.

[27]  H. Lode,et al.  Management of serious nosocomial bacterial infections: do current therapeutic options meet the need? , 2005, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[28]  M. Masnyk,et al.  Dirhodium tetraacetate as an auxiliary chromophore in a circular dichroic study on vic-amino alcohols , 2005 .

[29]  K. Anstrom,et al.  Staphylococcus aureus endocarditis: a consequence of medical progress. , 2005, JAMA.

[30]  S. Solomon,et al.  Methicillin-resistant–Staphylococcus aureus Hospitalizations, United States , 2005, Emerging infectious diseases.

[31]  D. M. Muñoz,et al.  Assembly intermediates in polyketide biosynthesis: enantioselective syntheses of beta-hydroxycarbonyl compounds. , 2005, Organic & biomolecular chemistry.

[32]  P. Schlievert,et al.  Virulence regulation in Staphylococcus aureus: the need for in vivo analysis of virulence factor regulation. , 2004, FEMS immunology and medical microbiology.

[33]  M. N. Reddy,et al.  Toward homogeneity of chirality via selective formation of homochiral or heterochiral aggregates. , 2004, Organic letters.

[34]  R. Novick Autoinduction and signal transduction in the regulation of staphylococcal virulence , 2003, Molecular microbiology.

[35]  C. Holmquist,et al.  A selective method for the direct conversion of aldehydes into .beta.-keto esters with ethyl diazoacetate catalyzed by tin(II) chloride , 1989 .

[36]  M. Braun,et al.  Stereoselektive Aldolreaktionen mit (R)‐ und (S)‐(2‐Hydroxy‐1,2,2‐triphenylethyl)acetat und verwandten Glycolmonoacetaten , 1988 .

[37]  M. Hiramoto,et al.  The structure of viscosin, a peptide antibiotic. I. Syntheses of D- and L-3-hydroxyacyl-L-leucine hydrazides related to viscosin. , 1971, Chemical & pharmaceutical bulletin.

[38]  G. Marshall,et al.  The biology and future prospects of antivirulence therapies , 2008, Nature Reviews Microbiology.

[39]  M. O'Reilly,et al.  Regulation of exoprotein gene expression in Staphylococcus aureus by agr , 2004, Molecular and General Genetics MGG.

[40]  F. Tenover,et al.  Staphylococcus aureus with reduced susceptibility to vancomycin isolated from a patient with fatal bacteremia. , 1999, Emerging infectious diseases.

[41]  A. Bernardi,et al.  Ethyl-(r)-(4-methylphenylsulfinyl)-n-methoxy acetimidate a useful chiral acetate equivalent in aldol type condensations , 1984 .