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Riluzole antagonizes the anxiogenic properties of the β-carboline FG 7142 in rats

Psychopharmacologia, 1989-01, Vol.99 (4), p.515-519

1989

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Structural and functional studies of cyclodipeptide synthases with RNA microhelices mimicking their tRNA susbtrates

Acta crystallographica. Section A, Foundations and advances, 2022-08, Vol.78 (a2), p.e344-e344

2022

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Genetic Identification of the Main Opportunistic Mucorales by PCR-Restriction Fragment Length Polymorphism

Journal of Clinical Microbiology, 2006-03, Vol.44 (3), p.805-810

2006

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Localization and Quantification of Carbon-Centered Radicals on Any Amino Acid of a Protein

Analytical chemistry (Washington), 2007-07, Vol.79 (14), p.5444-5448

2007

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Preparation of Chiral 2-Stannyloxazolidines and First Considerations on the Transacetalisation Reaction Mechanism

European journal of organic chemistry, 2004-10, Vol.2004 (20), p.4251-4267

2004

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Diastereoselective synthesis of chiral α-aminoorganotributyltins via ring-opening of 2-tributylstannyloxazolidines

Journal of organometallic chemistry, 2006-04, Vol.691 (8), p.1488-1497

2006

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Footprinting of Protein Interactions by Tritium Labeling

Biochemistry (Easton), 2010-05, Vol.49 (20), p.4297-4299

2010

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Identification of Chiral cis- and trans-2-Stannyloxazolidines by Their NMR Spectra and Solid-State Structures

European journal of organic chemistry, 2004-10, Vol.2004 (20), p.4268-4279

2004

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An Isosparteine Derivative for Stereochemical Assignment of Stereogenic (Chiral) Methyl Groups Using Tritium NMR: Theory and Experiment

Journal of the American Chemical Society, 2005-01, Vol.127 (1), p.412-420

2005

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The Shortest Route to Chiral Ditosylmethylamine

Angewandte Chemie International Edition, 2002-02, Vol.41 (3), p.497-498

2002

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Diastereoselective Synthesis of Chiral α-Aminoorganotins via Ring-Opening of Tributylstannyloxazolidines

Journal of organometallic chemistry, 2005

2005

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An alternative route to enantioenriched α-alkoxyalkylstannanes by stereoselective opening of chiral α-stannylacetals with organometallic reagents

Tetrahedron, 1997-06, Vol.53 (22), p.7615-7628

1997

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Stereoselective opening of chiral α-stannylacetals with organometallic reagents

Journal of organometallic chemistry, 1992-09, Vol.437 (1), p.C19-C22

1992

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ChemInform Abstract: An Alternative Route to Enantioenriched α-Alkoxyalkylstannanes by Stereoselective Opening of Chiral α-Stannylacetals with Organometallic Reagents

ChemInform, 1997-09, Vol.28 (40), p.no-no

1997

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ChemInform Abstract: Stereoselective Opening of Chiral α-Stannylacetals with Organometallic Reagents

ChemInform, 1993-01, Vol.24 (2), p.no-no

1993

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ChemInform Abstract: Diethoxymethyllithium: Generation via Transmetalation of Diethoxymethyltributyltin, Stability, Nucleophilic Reactivity in Addition Reactions, and Use as a Precursor of Group 14 Formylmetals

ChemInform, 1994-09, Vol.25 (38), p.no-no

1994

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Riluzole antagonizes the anxiogenic properties of the β-carboline FG 7142 in rats

Structural and functional studies of cyclodipeptide synthases with RNA microhelices mimicking their tRNA susbtrates

Genetic Identification of the Main Opportunistic Mucorales by PCR-Restriction Fragment Length Polymorphism

Localization and Quantification of Carbon-Centered Radicals on Any Amino Acid of a Protein

Preparation of Chiral 2-Stannyloxazolidines and First Considerations on the Transacetalisation Reaction Mechanism

Diastereoselective synthesis of chiral α-aminoorganotributyltins via ring-opening of 2-tributylstannyloxazolidines

Footprinting of Protein Interactions by Tritium Labeling

Identification of Chiral cis- and trans-2-Stannyloxazolidines by Their NMR Spectra and Solid-State Structures

An Isosparteine Derivative for Stereochemical Assignment of Stereogenic (Chiral) Methyl Groups Using Tritium NMR: Theory and Experiment

The Shortest Route to Chiral Ditosylmethylamine

Diastereoselective Synthesis of Chiral α-Aminoorganotins via Ring-Opening of Tributylstannyloxazolidines

An alternative route to enantioenriched α-alkoxyalkylstannanes by stereoselective opening of chiral α-stannylacetals with organometallic reagents

Stereoselective opening of chiral α-stannylacetals with organometallic reagents

ChemInform Abstract: An Alternative Route to Enantioenriched α-Alkoxyalkylstannanes by Stereoselective Opening of Chiral α-Stannylacetals with Organometallic Reagents

ChemInform Abstract: Stereoselective Opening of Chiral α-Stannylacetals with Organometallic Reagents

ChemInform Abstract: Diethoxymethyllithium: Generation via Transmetalation of Diethoxymethyltributyltin, Stability, Nucleophilic Reactivity in Addition Reactions, and Use as a Precursor of Group 14 Formylmetals

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