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Mild chemo-selective hydration of terminal alkynes catalysed by AgSbF6

Chemical communications (Cambridge, England), 2012-01, Vol.48 (3), p.434-436

2012

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Hydroformylation of Homoallylic Azides: A Rapid Approach toward Alkaloids

Organic letters, 2009-01, Vol.11 (2), p.261-264

2009

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Short Access to (+)-Lupinine and (+)-Epiquinamide via Double Hydroformylation

Organic letters, 2010-02, Vol.12 (3), p.528-531

2010

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Cyclohydrocarbonylation-Based Strategy toward Poly- Substituted Piperidines

Organic letters, 2011-05, Vol.13 (9), p.2294-2297

2011

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MRT‐92 inhibits Hedgehog signaling by blocking overlapping binding sites in the transmembrane domain of the Smoothened receptor

The FASEB journal, 2015-05, Vol.29 (5), p.1817-1829

2015

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Four-Component Reactions toward Fused Heterocyclic Rings

Organic letters, 2009-11, Vol.11 (22), p.5314-5317

2009

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Stereoselective Multicomponent Assembly of Enantiopure Oxazolopiperidines and -azepines

Journal of organic chemistry, 2012-03, Vol.77 (5), p.2246-2253

2012

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Hedgehog associated to microparticles inhibits adipocyte differentiation via a non-canonical pathway

Scientific reports, 2016-03, Vol.6 (1), p.23479-23479, Article 23479

2016

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Design, synthesis and biological characterization of a new class of osteogenic (1H)-quinolone derivatives

European journal of medicinal chemistry, 2016-10, Vol.121, p.747-757

2016

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Synthesis and biological evaluation of desmethylveramiline, a micromolar Hedgehog inhibitor

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (12), p.3608-3612

2011

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Virtual screening-based discovery and mechanistic characterization of the acylthiourea MRT-10 family as smoothened antagonists

Molecular pharmacology, 2010-10, Vol.78 (4), p.658-665

2010

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Discovery, molecular and pharmacological characterization of GSA-10, a novel small-molecule positive modulator of Smoothened

Molecular pharmacology, 2013-05, Vol.83 (5), p.1020-1029

2013

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Microwave-Assisted Domino Hydroformylation without Syngas

Synlett, 2011, Vol.2011 (2), p.199-202

2011

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Rhodium-catalyzed multicomponent synthesis of chiral oxazolopiperidines

Tetrahedron, 2010-05, Vol.66 (21), p.3749-3753

2010

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Identification and mechanism of action of the acylguanidine MRT-83, a novel potent Smoothened antagonist

Molecular pharmacology, 2011-03, Vol.79 (3), p.453-460

2011

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Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process

Chemical communications (Cambridge, England), 2014-09, Vol.50 (68), p.9657-9660

2014

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Microwave assisted hydroaminomethylation of alkenes

Tetrahedron letters, 2007-11, Vol.48 (48), p.8501-8504

2007

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Expeditious Route Towards (±)-Desethyleburnamonine, a Precursor of (±)-Vindeburnol

European Journal of Organic Chemistry, 2011-11, Vol.2011 (32), p.6409-6412

2011

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Microwaves Make Hydroformylation a Rapid and Easy Process

Organic letters, 2006-08, Vol.8 (17), p.3725-3727

2006

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1,2-Diastereoselective C-C Bond-Forming Reactions for the Synthesis of Chiral β-Branched α-Amino Acids

European Journal of Organic Chemistry, 2010-11, Vol.2010 (31), p.6005-6018

2010

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Hydroformylation of Alkenylamines. Concise Approaches toward Piperidines, Quinolizidines, and Related Alkaloids

Journal of organic chemistry, 2010-12, Vol.75 (24), p.8670-8673

2010

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Acylthiourea, Acylurea, and Acylguanidine Derivatives with Potent Hedgehog Inhibiting Activity

Journal of medicinal chemistry, 2012-02, Vol.55 (4), p.1559-1571

2012

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A New Method for the Synthesis of Chiral β-Branched α-Amino Acids

Organic letters, 2007-09, Vol.9 (20), p.3881-3884

2007

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Identification of a low-molecular weight TrkB antagonist with anxiolytic and antidepressant activity in mice

The Journal of clinical investigation, 2011-05, Vol.121 (5), p.1846-1857

2011

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From the Promiscuous Asenapine to Potent Fluorescent Ligands Acting at a Series of Aminergic G‑Protein-Coupled Receptors

Journal of medicinal chemistry, 2018-01, Vol.61 (1), p.174-188

2018

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Mild chemo-selective hydration of terminal alkynes catalysed by AgSbF6

Hydroformylation of Homoallylic Azides: A Rapid Approach toward Alkaloids

Short Access to (+)-Lupinine and (+)-Epiquinamide via Double Hydroformylation

Cyclohydrocarbonylation-Based Strategy toward Poly- Substituted Piperidines

MRT‐92 inhibits Hedgehog signaling by blocking overlapping binding sites in the transmembrane domain of the Smoothened receptor

Four-Component Reactions toward Fused Heterocyclic Rings

Stereoselective Multicomponent Assembly of Enantiopure Oxazolopiperidines and -azepines

Hedgehog associated to microparticles inhibits adipocyte differentiation via a non-canonical pathway

Design, synthesis and biological characterization of a new class of osteogenic (1H)-quinolone derivatives

Synthesis and biological evaluation of desmethylveramiline, a micromolar Hedgehog inhibitor

Virtual screening-based discovery and mechanistic characterization of the acylthiourea MRT-10 family as smoothened antagonists

Discovery, molecular and pharmacological characterization of GSA-10, a novel small-molecule positive modulator of Smoothened

Microwave-Assisted Domino Hydroformylation without Syngas

Rhodium-catalyzed multicomponent synthesis of chiral oxazolopiperidines

Identification and mechanism of action of the acylguanidine MRT-83, a novel potent Smoothened antagonist

Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process

Microwave assisted hydroaminomethylation of alkenes

Expeditious Route Towards (±)-Desethyleburnamonine, a Precursor of (±)-Vindeburnol

Microwaves Make Hydroformylation a Rapid and Easy Process

1,2-Diastereoselective C-C Bond-Forming Reactions for the Synthesis of Chiral β-Branched α-Amino Acids

Hydroformylation of Alkenylamines. Concise Approaches toward Piperidines, Quinolizidines, and Related Alkaloids

Acylthiourea, Acylurea, and Acylguanidine Derivatives with Potent Hedgehog Inhibiting Activity

A New Method for the Synthesis of Chiral β-Branched α-Amino Acids

Identification of a low-molecular weight TrkB antagonist with anxiolytic and antidepressant activity in mice

From the Promiscuous Asenapine to Potent Fluorescent Ligands Acting at a Series of Aminergic G‑Protein-Coupled Receptors

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