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Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (-)-nicotlactone B and (-)-galbacin

Organic & biomolecular chemistry, 2018-03, Vol.16 (10), p.1672-1678

2018

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Structural and molecular bases to IRE1 activity modulation

Biochemical journal, 2021-08, Vol.478 (15), p.2953-2975

2021

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Synthesis and evaluation of new ω-borono-α-amino acids as rat liver arginase inhibitors

Bioorganic & medicinal chemistry, 2005-04, Vol.13 (7), p.2373-2379

2005

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The Allyl Cyanate/Isocyanate Rearrangement: An Efficient Tool for the Stereocontrolled Formation of Allylic C–N Bonds

European journal of organic chemistry, 2017-03, Vol.2017 (10), p.1295-1307

2017

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Stereospecific Synthesis of α‑Amino Allylsilane Derivatives through a [3,3]-Allyl Cyanate Rearrangement. Mild Formation of Functionalized Disiloxanes

Journal of organic chemistry, 2016-06, Vol.81 (11), p.4633-4644

2016

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N-Benzylpolyamines as Vectors of Boron and Fluorine for Cancer Therapy and Imaging: Synthesis and Biological Evaluation

Journal of medicinal chemistry, 2001-10, Vol.44 (22), p.3653-3664

2001

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Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (−)-nicotlactone B and (−)-galbacinElectronic supplementary information (ESI) available: Characterization and NMR spectra of all compounds. DFT and computational data. CCDC 1578065. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob00101d

2018-03

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P.1.c.014 - Inhibition of DYRK1A overdosage restores cognition in Down syndrome models through DYRK1A-interaction with major players of synaptic transmission

European neuropsychopharmacology, 2017-10, Vol.27, p.S611-S612

2017

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Inhibition of DYRK1A overdosage restores cognition in Down syndrome models through DYRK1A-interaction with major players of synaptic transmission

European neuropsychopharmacology, 2017-10, Vol.27, p.S611-S612

2017

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A stereoselective route to 3-methyl-2-methylsulfanyl-5-ylidene-3,5-dihydroimidazol-4-one derivatives and precursor of Leucettamine B

Green chemistry : an international journal and green chemistry resource : GC, 2001, Vol.3 (4), p.165-169

2001

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Catalytic Enantioselective Three-Component Hetero-[4+2] Cycloaddition/Allylboration Approach to α-Hydroxyalkyl Pyrans: Scope, Limitations, and Mechanistic Proposal

Chemistry : a European journal, 2006-04, Vol.12 (11), p.3132-3142

2006

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Efficient Asymmetric Synthesis of 2,6-Disubstituted 2H-Dihydropyrans via a Catalytic Hetero-Diels-Alder/Allylboration Sequence

Advanced synthesis & catalysis, 2003-11, Vol.345 (11), p.1215-1219

2003

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Metal-Catalyzed Release of Supported Boronic Acids for C−C Bond Formation

Organic letters, 2001-03, Vol.3 (6), p.803-805

2001

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A Concise Synthesis of (+)-Goniodiol Using a Catalytic Hetero Diels-Alder/Allylboration Sequence

Synlett, 2005-06, Vol.2005 (9), p.1462-1464

2005

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Ruthenium-catalyzed tandem allylic substitution/isomerization: a direct route to propiophenones from cinnamyl chloride derivatives

New journal of chemistry, 2008-01, Vol.32 (6), p.929-931

2008

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Reactivity of 2-thiohydantoins towards various electrophilic reagents: applications to the synthesis of new 2-ylidene-3,5-dihydro-4H-imidazol-4-ones

Molecules (Basel, Switzerland), 2004-09, Vol.9 (10), p.867-875

2004

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Tartaric Acid Derived Aziridines as Chiral Precursors of 3-Amino-3-deoxy and 2-Amino-2-deoxy Tetroses: An Efficient Approach Towards Mugineic Acid

Synlett, 1992, Vol.1992 (6), p.527-529

1992

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Boronic ester as a linker system for solid phase synthesis

Tetrahedron letters, 1999-11, Vol.40 (45), p.7979-7983

1999

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Microwave-mediated solventless synthesis of new derivatives of marine alkaloid Leucettamine B

Tetrahedron letters, 2002-05, Vol.43 (19), p.3581-3584

2002

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[4+3] versus [4+2] Mechanisms in the Dimerization of 2-Boryl-1,3-butadienes. A Theoretical and Experimental Study

Journal of organic chemistry, 2002-12, Vol.67 (26), p.9153-9161

2002

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Boronate linker for ‘traceless’ solid-phase synthesis

Chemical communications (Cambridge, England), 2000-01 (14), p.1275-1276

2000

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A practical and eco-friendly synthesis of stereocontrolled alkylaminomethylidene derivatives of 2-thiohydantoins by dimethylamine substitution

Tetrahedron letters, 2002-11, Vol.43 (48), p.8745-8749

2002

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Enantiospecific Synthesis of Polyoxamic Acid from L-Arabinose

Synthesis (Stuttgart), 1991, Vol.1991 (2), p.150-155

1991

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An enantiospecific synthesis of polyoxamic acid from L-arabinose

Tetrahedron letters, 1989, Vol.30 (34), p.4527-4530

1989

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Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (-)-nicotlactone B and (-)-galbacin

Structural and molecular bases to IRE1 activity modulation

Synthesis and evaluation of new ω-borono-α-amino acids as rat liver arginase inhibitors

The Allyl Cyanate/Isocyanate Rearrangement: An Efficient Tool for the Stereocontrolled Formation of Allylic C–N Bonds

Stereospecific Synthesis of α‑Amino Allylsilane Derivatives through a [3,3]-Allyl Cyanate Rearrangement. Mild Formation of Functionalized Disiloxanes

N-Benzylpolyamines as Vectors of Boron and Fluorine for Cancer Therapy and Imaging: Synthesis and Biological Evaluation

P.1.c.014 - Inhibition of DYRK1A overdosage restores cognition in Down syndrome models through DYRK1A-interaction with major players of synaptic transmission

Inhibition of DYRK1A overdosage restores cognition in Down syndrome models through DYRK1A-interaction with major players of synaptic transmission

A stereoselective route to 3-methyl-2-methylsulfanyl-5-ylidene-3,5-dihydroimidazol-4-one derivatives and precursor of Leucettamine B

Catalytic Enantioselective Three-Component Hetero-[4+2] Cycloaddition/Allylboration Approach to α-Hydroxyalkyl Pyrans: Scope, Limitations, and Mechanistic Proposal

Efficient Asymmetric Synthesis of 2,6-Disubstituted 2H-Dihydropyrans via a Catalytic Hetero-Diels-Alder/Allylboration Sequence

Metal-Catalyzed Release of Supported Boronic Acids for C−C Bond Formation

A Concise Synthesis of (+)-Goniodiol Using a Catalytic Hetero Diels-Alder/Allylboration Sequence

Ruthenium-catalyzed tandem allylic substitution/isomerization: a direct route to propiophenones from cinnamyl chloride derivatives

Reactivity of 2-thiohydantoins towards various electrophilic reagents: applications to the synthesis of new 2-ylidene-3,5-dihydro-4H-imidazol-4-ones

Cross Coupling and Heck-Type Reactions 1: C-C Cross Coupling Using Organometallic Partners

Tartaric Acid Derived Aziridines as Chiral Precursors of 3-Amino-3-deoxy and 2-Amino-2-deoxy Tetroses: An Efficient Approach Towards Mugineic Acid

Boronic ester as a linker system for solid phase synthesis

Microwave-mediated solventless synthesis of new derivatives of marine alkaloid Leucettamine B

[4+3] versus [4+2] Mechanisms in the Dimerization of 2-Boryl-1,3-butadienes. A Theoretical and Experimental Study

Boronate linker for ‘traceless’ solid-phase synthesis

A practical and eco-friendly synthesis of stereocontrolled alkylaminomethylidene derivatives of 2-thiohydantoins by dimethylamine substitution

Enantiospecific Synthesis of Polyoxamic Acid from L-Arabinose

An enantiospecific synthesis of polyoxamic acid from L-arabinose

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