Lista de obras - Guido Sello - Dominio Público Uruguay

(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric Reformatsky reactions

1,2-Dihydro-1,2-dihydroxynaphthalene dehydrogenase containing recombinant strains: Preparation, isolation and characterisation of 1,2-dihydroxynaphthalenes and 1,2-naphthoquinones

A chemoenzymatic synthesis of (2R)-8-substituted-2-aminotetralins

Aldol reactions of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) from Pseudomonas fluorescens N3.

artículo científico publicado en 2013

Analysis of a theoretical model based on similarity for studying RNA base pairings

scientific article published on 01 August 1996

Bacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: study of the effects of substituent nature and position

Biocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactions

Bioconversion of Substituted Naphthalenes to the Corresponding 1,2-Dihydroxy Derivatives by Escherichia coli Recombinant Strains

Carcinogenicity prediction of noncongeneric chemicals by augmented top priority fragment classification.

artículo científico publicado en 2016

Cathode and medium effects on the electroreductive glucosidation of phenols

Characterization of the aldol condensation activity of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) cloned from Pseudomonas fluorescens N3.

artículo científico publicado en 2011

Determination of toxicant mode of action by augmented top priority fragment class

artículo científico publicado en 2013

Development of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions

scientific article published on 01 June 2000

Electroreduction of volatile organic halides on activated silver cathodes

Enantiopure vic-amino alcohols and vic-diamines from (1R,2S)-1,2-dihydroxy-1,2-dihydronaphthalene

Formation of bound residues by naphthalene and cis-naphthalene-1,2-dihydrodiol.

artículo científico publicado en 2004

From dioxin to dioxin congeners: understanding the differences in hydrophobic aggregation in water and absorption into lipid membranes by means of atomistic simulations

artículo científico publicado en 2016

Hydrophobic aggregation and collective absorption of dioxin into lipid membranes: insights from atomistic simulations

artículo científico publicado en 2014

Identification of toxifying and detoxifying moieties for mutagenicity prediction by priority assessment

artículo científico publicado el 28 de junio de 2011

Insect pest control agents: Novel chiral butanoate esters (juvenogens)

article by Zdenek Wimmer et al published 15 September 2007 in Bioorganic & Medicinal Chemistry

Isolation, cloning and synthetic use of the tHBP aldolase from Pseudomonas fluorescens N3

Microbial enzymes for aromatic compound hydroxylation.

artículo científico publicado en 2011

Multienzymatic preparation of (−)-[3-(oxiran-2-yl)phenyl]methanol and (−)-3-(oxiran-2-yl)benzoic acid

Multienzymatic preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acid

Novel auto-inducing expression systems for the development of whole-cell biocatalysts.

artículo científico publicado en 2008

One-Pot Wittig Reactions in Water and in the Presence of a Surfactant

Organic phase effect in the biphasic bioconversion of substituted naphthalenes by engineered E. coli containing P. fluorescens N3 dioxygenase

Organization and regulation of meta cleavage pathway genes for toluene and o-xylene derivative degradation in Pseudomonas stutzeri OX1.

artículo científico publicado en 2001

Predicting toxicity: a mechanism of action model of chemical mutagenicity.

artículo científico publicado en 2001

Prediction of organic reaction products: determining the best reaction conditions

artículo científico publicado en 2000

Production of substituted naphthalene dihydrodiols by engineered Escherichia coli containing the cloned naphthalene 1,2-dioxygenase gene from Pseudomonas fluorescens N3.

artículo científico publicado en 1997

Reaction centre accessibility. I. Calculation of reaction centre congestion and influence of structure flexibility

artículo científico publicado en 2000

Reaction centre accessibility. II. Role of reaction centre congestion in the calculation of reaction centre accessibility

artículo científico publicado en 2000

Regulated expression systems for the development of whole-cell biocatalysts expressing oxidative enzymes in a sequential manner.

artículo científico publicado en 2013

Selective enzymatic reduction of aldehydes.

artículo científico publicado en 2006

Silver as a powerful electrocatalyst for organic halide reduction: the critical role of molecular structure

Specificity of substrate recognition by Pseudomonas fluorescens N3 dioxygenase. The role of the oxidation potential and molecular geometry

artículo científico publicado en 1997

Styrene lower catabolic pathway in Pseudomonas fluorescens ST: identification and characterization of genes for phenylacetic acid degradation.

artículo científico publicado en 2007

Synthesis and biological evaluation of new 3-amino-2-azetidinone derivatives as anti-colorectal cancer agents.

artículo científico publicado en 2018

Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio- and diastereoselective chemical aminolysis

article published in 2006

Top-priority fragment QSAR approach in predicting pesticide aquatic toxicity

artículo científico publicado en 2006

Lista de obras de Guido Sello

(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric Reformatsky reactions

1,2-Dihydro-1,2-dihydroxynaphthalene dehydrogenase containing recombinant strains: Preparation, isolation and characterisation of 1,2-dihydroxynaphthalenes and 1,2-naphthoquinones

A chemoenzymatic synthesis of (2R)-8-substituted-2-aminotetralins

Aldol reactions of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) from Pseudomonas fluorescens N3.

Analysis of a theoretical model based on similarity for studying RNA base pairings

Bacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: study of the effects of substituent nature and position

Biocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactions

Bioconversion of Substituted Naphthalenes to the Corresponding 1,2-Dihydroxy Derivatives by Escherichia coli Recombinant Strains

Carcinogenicity prediction of noncongeneric chemicals by augmented top priority fragment classification.

Cathode and medium effects on the electroreductive glucosidation of phenols

Characterization of the aldol condensation activity of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) cloned from Pseudomonas fluorescens N3.

Determination of toxicant mode of action by augmented top priority fragment class

Development of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions

Electroreduction of volatile organic halides on activated silver cathodes

Enantiopure vic-amino alcohols and vic-diamines from (1R,2S)-1,2-dihydroxy-1,2-dihydronaphthalene

Formation of bound residues by naphthalene and cis-naphthalene-1,2-dihydrodiol.

From dioxin to dioxin congeners: understanding the differences in hydrophobic aggregation in water and absorption into lipid membranes by means of atomistic simulations

Hydrophobic aggregation and collective absorption of dioxin into lipid membranes: insights from atomistic simulations

Identification of toxifying and detoxifying moieties for mutagenicity prediction by priority assessment

Insect pest control agents: Novel chiral butanoate esters (juvenogens)

Isolation, cloning and synthetic use of the tHBP aldolase from Pseudomonas fluorescens N3

Microbial enzymes for aromatic compound hydroxylation.

Multienzymatic preparation of (−)-[3-(oxiran-2-yl)phenyl]methanol and (−)-3-(oxiran-2-yl)benzoic acid

Multienzymatic preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acid

Novel auto-inducing expression systems for the development of whole-cell biocatalysts.

One-Pot Wittig Reactions in Water and in the Presence of a Surfactant

Organic phase effect in the biphasic bioconversion of substituted naphthalenes by engineered E. coli containing P. fluorescens N3 dioxygenase

Organization and regulation of meta cleavage pathway genes for toluene and o-xylene derivative degradation in Pseudomonas stutzeri OX1.

Predicting toxicity: a mechanism of action model of chemical mutagenicity.

Prediction of organic reaction products: determining the best reaction conditions

Production of substituted naphthalene dihydrodiols by engineered Escherichia coli containing the cloned naphthalene 1,2-dioxygenase gene from Pseudomonas fluorescens N3.

Reaction centre accessibility. I. Calculation of reaction centre congestion and influence of structure flexibility

Reaction centre accessibility. II. Role of reaction centre congestion in the calculation of reaction centre accessibility

Regulated expression systems for the development of whole-cell biocatalysts expressing oxidative enzymes in a sequential manner.

Selective enzymatic reduction of aldehydes.

Silver as a powerful electrocatalyst for organic halide reduction: the critical role of molecular structure

Specificity of substrate recognition by Pseudomonas fluorescens N3 dioxygenase. The role of the oxidation potential and molecular geometry

Styrene lower catabolic pathway in Pseudomonas fluorescens ST: identification and characterization of genes for phenylacetic acid degradation.

Synthesis and biological evaluation of new 3-amino-2-azetidinone derivatives as anti-colorectal cancer agents.

Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio- and diastereoselective chemical aminolysis

Top-priority fragment QSAR approach in predicting pesticide aquatic toxicity