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Isolation of Picrotoxanes from Austrobuxus carunculatus Using Taxonomy-Based Molecular Networking

Journal of natural products (Washington, D.C.), 2020-10, Vol.83 (10), p.3069-3079

2020

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Molecular and cellular dissection of the oxysterol-binding protein cycle through a fluorescent inhibitor

The Journal of biological chemistry, 2020-03, Vol.295 (13), p.4277-4288

2020

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Synthesis and Anti-Leishmanial Properties of Quinolones Derived from Zanthosimuline

Molecules (Basel, Switzerland), 2022-11, Vol.27 (22), p.7892

2022

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NA1—115—7, from Zygogynum pancheri, is a new selective MCL-1 inhibitor inducing the apoptosis of hematological cancer cells but non-toxic to normal blood cells or cardiomyocytes

Biomedicine & pharmacotherapy, 2022-10, Vol.154, p.113546-113546, Article 113546

2022

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Characterization, Diversity, and Structure-Activity Relationship Study of Lipoamino Acids from Pantoea sp. and Synthetic Analogues

International journal of molecular sciences, 2019-03, Vol.20 (5), p.1083

2019

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Development of an efficient route toward meiogynin A-inspired dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

Organic & biomolecular chemistry, 2015-05, Vol.13 (19), p.5520-5531

2015

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A Fast and Efficient Molecular Networking Approach for Reactivity of Natural Products Exploration in Plant Extracts: Application to Diterpene Esters from Euphorbia dendroides

Journal of natural products (Washington, D.C.), 2024-06, Vol.87 (6), p.1574-1581

2024

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Selectivity in the Intermolecular Diels–Alder Reaction of Conjugated Trienes: Experimental and Theoretical Approaches

European journal of organic chemistry, 2018-11, Vol.2018 (42), p.5869-5877

2018

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Intramolecular Imino Diels−Alder Reaction: Progress toward the Synthesis of Uncialamycin

Journal of organic chemistry, 2009-09, Vol.74 (17), p.6728-6734

2009

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Development of an efficient route toward meiogynin A-inspired dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteinsElectronic supplementary information (ESI) available: 1H and 13C NMR spectra for all new compounds. See DOI: 10.1039/c5ob00354g

2015-05

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Structurally Diverse Diterpenoids from Sandwithia guyanensis

Journal of natural products (Washington, D.C.), 2018-04, Vol.81 (4), p.901-912

2018

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Dual inhibitors of the pro-survival proteins Bcl-2 and Mcl-1 derived from natural compound meiogynin A

European journal of medicinal chemistry, 2018-03, Vol.148, p.26-38

2018

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Structure-Based Design of a Lead Compound Derived from Natural Schweinfurthins with Antitumor Properties That Target Oxysterol-Binding Protein

Journal of medicinal chemistry, 2023-10, Vol.66 (20), p.14208-14220

2023

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From meiogynin A to the synthesis of dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

Chemical communications (Cambridge, England), 2014-08, Vol.50 (62), p.8593-8596

2014

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Pro-apoptotic carboxamide analogues of natural fislatifolic acid targeting Mcl-1 and Bcl-2

Bioorganic & medicinal chemistry letters, 2020-04, Vol.30 (7), p.127003-127003, Article 127003

2020

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Methylaluminoxane (MAO)-Assisted Direct Amidation of Esters

Synlett, 2015-02, Vol.26 (3), p.385-387

2015

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Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels-Alder and ene-reactionsElectronic supplementary information (ESI) available: Experimental procedures, NMR and crystallographic data. CCDC 1530223-1530226. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob01236e

2017-07

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Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels-Alder and ene-reactions

Organic & biomolecular chemistry, 2017, Vol.15 (26), p.5585-5592

2017

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Asymmetric Total Synthesis and Biological Evaluation of Proapoptotic Natural Myrcene‐Derived Cyclohexenyl Chalcones

European journal of organic chemistry, 2018-11, Vol.2018 (42), p.5830-5835

2018

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Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines

Organic Chemistry Frontiers, 2018-01, Vol.5 (14), p.2171-2178

2018

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Drimane Derivatives as the First Examples of Covalent BH3 Mimetics that Target MCL‐1

ChemMedChem, 2021-06, Vol.16 (11), p.1788-1797

2021

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Asymmetric Synthesis of Two Analogues of Meiogynin A

European journal of organic chemistry, 2013-04, Vol.2013 (11), p.2116-2122

2013

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Setbacks and hopes: en route to the synthesis of uncialamycin

Tetrahedron, 2011-09, Vol.67 (39), p.7510-7516

2011

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Taming the Carboxyl Group for Directed Carbometalation: Observations on the Use of Anions, Dianions and Ester Enolates

Chemistry : a European journal, 2014-07, Vol.20 (29), p.8918-8922

2014

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Ring-rearrangement metathesis of substituted dihydropyrans and dihydrofurans

Tetrahedron, 2011-01, Vol.67 (2), p.339-357

2011

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Isolation of Picrotoxanes from Austrobuxus carunculatus Using Taxonomy-Based Molecular Networking

Molecular and cellular dissection of the oxysterol-binding protein cycle through a fluorescent inhibitor

Synthesis and Anti-Leishmanial Properties of Quinolones Derived from Zanthosimuline

NA1—115—7, from Zygogynum pancheri, is a new selective MCL-1 inhibitor inducing the apoptosis of hematological cancer cells but non-toxic to normal blood cells or cardiomyocytes

Characterization, Diversity, and Structure-Activity Relationship Study of Lipoamino Acids from Pantoea sp. and Synthetic Analogues

Development of an efficient route toward meiogynin A-inspired dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

A Fast and Efficient Molecular Networking Approach for Reactivity of Natural Products Exploration in Plant Extracts: Application to Diterpene Esters from Euphorbia dendroides

Selectivity in the Intermolecular Diels–Alder Reaction of Conjugated Trienes: Experimental and Theoretical Approaches

Intramolecular Imino Diels−Alder Reaction: Progress toward the Synthesis of Uncialamycin

Development of an efficient route toward meiogynin A-inspired dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteinsElectronic supplementary information (ESI) available: 1H and 13C NMR spectra for all new compounds. See DOI: 10.1039/c5ob00354g

Structurally Diverse Diterpenoids from Sandwithia guyanensis

Dual inhibitors of the pro-survival proteins Bcl-2 and Mcl-1 derived from natural compound meiogynin A

Structure-Based Design of a Lead Compound Derived from Natural Schweinfurthins with Antitumor Properties That Target Oxysterol-Binding Protein

From meiogynin A to the synthesis of dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

Pro-apoptotic carboxamide analogues of natural fislatifolic acid targeting Mcl-1 and Bcl-2

Methylaluminoxane (MAO)-Assisted Direct Amidation of Esters

Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels-Alder and ene-reactions

Asymmetric Total Synthesis and Biological Evaluation of Proapoptotic Natural Myrcene‐Derived Cyclohexenyl Chalcones

Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines

Drimane Derivatives as the First Examples of Covalent BH3 Mimetics that Target MCL‐1

Asymmetric Synthesis of Two Analogues of Meiogynin A

Setbacks and hopes: en route to the synthesis of uncialamycin

Taming the Carboxyl Group for Directed Carbometalation: Observations on the Use of Anions, Dianions and Ester Enolates

Ring-rearrangement metathesis of substituted dihydropyrans and dihydrofurans

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