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Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry

Chemical reviews, 2016-12, Vol.116 (24), p.15235-15283

2016

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Metal complexes as a promising source for new antibiotics

Chemical science (Cambridge), 2020-03, Vol.11 (1), p.2627-2639

2020

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Enantioselective Ruthenium-Catalyzed 1,3-Dipolar Cycloadditions between C‑Carboalkoxy Ketonitrones and Methacrolein: Solvent Effect on Reaction Selectivity and Its Rational

Journal of organic chemistry, 2014-04, Vol.79 (8), p.3414-3426

2014

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Hetero-Diels−Alder Reactions of Cyclic Ketone Derived Enamide. A New and Efficient Concept for the Asymmetric Robinson Annulation

Organic letters, 2009-07, Vol.11 (14), p.3060-3063

2009

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1,3-Dipolar Cycloaddition of N-Substituted Dipolarophiles and Nitrones: Highly Efficient Solvent-Free Reaction

Journal of organic chemistry, 2008-04, Vol.73 (7), p.2621-2632

2008

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Stereodivergent approach in the protected glycal synthesis of L-vancosamine, L-saccharosamine, L-daunosamine and L-ristosamine involving a ring-closing metathesis step

Beilstein journal of organic chemistry, 2018-11, Vol.14 (1), p.2949-2955

2018

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Organocatalytic enantio- and diastereoselective 1,3-dipolar cycloaddition between alanine-derived ketonitrones and E-crotonaldehyde: efficiency and full stereochemical studies

Tetrahedron: asymmetry, 2012-12, Vol.23 (24), p.1670-1677

2012

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Enantioselective Access to Robinson Annulation Products and Michael Adducts as Precursors

Angewandte Chemie International Edition, 2017-10, Vol.56 (41), p.12424-12458

International ed. in English, 2017

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1,3-Dipolar Cycloadditions of Nitrones to Heterosubstituted Alkenes. Part 1: Oxa and Aza-substituted Alkenes

Organic preparations and procedures international, 2010-10, Vol.42 (5), p.387-431

2010

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N-(β,β-Difluorovinyl)oxazolidin-2-ones: First Synthesis and Application in [3+2]- and [4+2]-Cycloaddition-Type Reactions

Synlett, 2009-09, Vol.2009 (15), p.2492-2496

2009

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N-Vinyl-2-oxazolidinones: Efficient Chiral Dienophiles for the [4 + 2]-Based de Novo Synthesis of New N-2-Deoxyglycosides

Journal of organic chemistry, 2004-06, Vol.69 (12), p.4192-4202

2004

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Glycosidations of 2-deoxy glycosyl dithiophosphates using a tagged iodine(III)-promoter for simple purification

Organic & biomolecular chemistry, 2008-01, Vol.6 (5), p.893-898

2008

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Stereospecific C‐Glycosylation by Mizoroki–Heck Reaction: A Powerful and Easy‐to‐Set‐Up Synthetic Tool to Access α‐ and β‐Aryl‐C‐Glycosides

Chemistry : a European journal, 2018-09, Vol.24 (53), p.14069-14074

2018

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Synthesis of Constrained C‐Glycosyl Amino Acid Derivatives Involving 1,3‐Dipolar Cycloaddition of Cyclic Nitrone as Key Step

European journal of organic chemistry, 2020-11, Vol.2020 (43), p.6749-6757

2020

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δ‑Valerolactamic Quaternary Amino Acid Derivatives: Enantiodivergent Synthesis and Evidence for Stereodifferentiated β‑Turn-Inducing Properties

Journal of organic chemistry, 2021-06, Vol.86 (12), p.8041-8055

2021

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MgI 2 ‐Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies

Chemistry : a European journal, 2015-07, Vol.21 (31), p.11014-11016

2015

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TIPS-Diazoacetone Aldol Addition: Mechanistic Aspects and Contribution to the Synthesis

Journal of organic chemistry, 2021-04, Vol.86 (7), p.4917-4931

2021

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MgI sub(2)-Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies

Chemistry : a European journal, 2015-07, Vol.21 (31), p.11014-11016

2015

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New N-Substituted Dipolarophiles in 1,3-Dipolar Cycloaddition of Nitrones

Synlett, 2006-12, Vol.2006 (19), p.3255-3258

2006

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Stereospecific C‐Glycosylation by Mizoroki–Heck Reaction: APowerful and Easy‐to‐Set‐Up Synthetic Tool to Access α‐ and β‐Aryl‐C‐Glycosides

Chemistry : a European journal, 2018-09, Vol.24 (53), p.14069-14074

2018

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TBAF-Triggered Aldol-Type Addition of α‑Triethylsilyl-α-diazoacetone

Journal of organic chemistry, 2015-10, Vol.80 (20), p.9980-9988

2015

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MgI2-Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies

Chemistry : a European journal, 2015-07, Vol.21 (31), p.11014-11016

2015

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Synthesis of Polysubstituted Pyrroles

Letters in organic chemistry, 2009-07, Vol.6 (5), p.359-361

2009

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Acetylene-free synthesis of vinyloxy pyridine and quinoline

Tetrahedron letters, 2016-12, Vol.57 (51), p.5825-5829

2016

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Reaction of Glyconitriles with Organometallic Reagents: Access to Acyl β‑C‑Glycosides

Journal of organic chemistry, 2016-03, Vol.81 (6), p.2364-2371

2016

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Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry

Metal complexes as a promising source for new antibiotics

Enantioselective Ruthenium-Catalyzed 1,3-Dipolar Cycloadditions between C‑Carboalkoxy Ketonitrones and Methacrolein: Solvent Effect on Reaction Selectivity and Its Rational

Hetero-Diels−Alder Reactions of Cyclic Ketone Derived Enamide. A New and Efficient Concept for the Asymmetric Robinson Annulation

1,3-Dipolar Cycloaddition of N-Substituted Dipolarophiles and Nitrones: Highly Efficient Solvent-Free Reaction

Stereodivergent approach in the protected glycal synthesis of L-vancosamine, L-saccharosamine, L-daunosamine and L-ristosamine involving a ring-closing metathesis step

Organocatalytic enantio- and diastereoselective 1,3-dipolar cycloaddition between alanine-derived ketonitrones and E-crotonaldehyde: efficiency and full stereochemical studies

Enantioselective Access to Robinson Annulation Products and Michael Adducts as Precursors

1,3-Dipolar Cycloadditions of Nitrones to Heterosubstituted Alkenes. Part 1: Oxa and Aza-substituted Alkenes

N-(β,β-Difluorovinyl)oxazolidin-2-ones: First Synthesis and Application in [3+2]- and [4+2]-Cycloaddition-Type Reactions

N-Vinyl-2-oxazolidinones: Efficient Chiral Dienophiles for the [4 + 2]-Based de Novo Synthesis of New N-2-Deoxyglycosides

Glycosidations of 2-deoxy glycosyl dithiophosphates using a tagged iodine(III)-promoter for simple purification

Stereospecific C‐Glycosylation by Mizoroki–Heck Reaction: A Powerful and Easy‐to‐Set‐Up Synthetic Tool to Access α‐ and β‐Aryl‐C‐Glycosides

Synthesis of Constrained C‐Glycosyl Amino Acid Derivatives Involving 1,3‐Dipolar Cycloaddition of Cyclic Nitrone as Key Step

δ‑Valerolactamic Quaternary Amino Acid Derivatives: Enantiodivergent Synthesis and Evidence for Stereodifferentiated β‑Turn-Inducing Properties

MgI 2 ‐Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies

TIPS-Diazoacetone Aldol Addition: Mechanistic Aspects and Contribution to the Synthesis

MgI sub(2)-Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies

New N-Substituted Dipolarophiles in 1,3-Dipolar Cycloaddition of Nitrones

Stereospecific C‐Glycosylation by Mizoroki–Heck Reaction: APowerful and Easy‐to‐Set‐Up Synthetic Tool to Access α‐ and β‐Aryl‐C‐Glycosides

TBAF-Triggered Aldol-Type Addition of α‑Triethylsilyl-α-diazoacetone

MgI2-Mediated Chemoselective Cleavage of Protecting Groups: An Alternative to Conventional Deprotection Methodologies

Synthesis of Polysubstituted Pyrroles

Acetylene-free synthesis of vinyloxy pyridine and quinoline

Reaction of Glyconitriles with Organometallic Reagents: Access to Acyl β‑C‑Glycosides

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