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Selective autoxidation of benzylamines: application to the synthesis of some nitrogen heterocycles

Green chemistry : an international journal and green chemistry resource : GC, 2013-01, Vol.15 (10), p.2713-2717

2013

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Toward the Synthesis of Sceptrin and Benzosceptrin: Solvent Effect in Stereo‐ and Regioselective [2+2] Photodimerization and Easy Access to the Fully Substituted Benzobutane

European journal of organic chemistry, 2018-11, Vol.2018 (42), p.5861-5868

2018

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Unaromatized Tetrahydrobenzimidazole Synthesis from p‐Benzoquinone and N‐Arylamidines and their Cytotoxic Potential

European journal of organic chemistry, 2018-11, Vol.2018 (42), p.5878-5884

2018

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Short‐Cut Bio‐Inspired Synthesis of Tricyclic Guanidinic Motifs of Crambescidins and Batzelladines Marine Alkaloids

European journal of organic chemistry, 2020-09, Vol.2020 (35), p.5677-5684

2020

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Tetrahydrobenzimidazole TMQ0153 triggers apoptosis, autophagy and necroptosis crosstalk in chronic myeloid leukemia

Cell death & disease, 2020-02, Vol.11 (2), p.109, Article 109

2020

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Elemental Sulfur Disproportionation in the Redox Condensation Reaction between o-Halonitrobenzenes and Benzylamines

Angewandte Chemie (International ed.), 2014-12, Vol.53 (50), p.13808-13812

International ed. in English, 2014

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Nitro-Methyl Redox Coupling: Efficient Approach to 2‑Hetarylbenzothiazoles from 2‑Halonitroarene, Methylhetarene, and Elemental Sulfur

Organic letters, 2013-08, Vol.15 (16), p.4218-4221

2013

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Three-Component Reaction between Alkynes, Elemental Sulfur, and Aliphatic Amines: A General, Straightforward, and Atom Economical Approach to Thioamides

Organic letters, 2014-01, Vol.16 (1), p.310-313

2014

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Benzazoles from Aliphatic Amines and o‑Amino/Mercaptan/Hydroxyanilines: Elemental Sulfur as a Highly Efficient and Traceless Oxidizing Agent

Organic letters, 2012-12, Vol.14 (23), p.5948-5951

2012

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Sodium Sulfide: A Sustainable Solution for Unbalanced Redox Condensation Reaction between o-Nitroanilines and Alcohols Catalyzed by an Iron–Sulfur System

Synthesis (Stuttgart), 2015-06, Vol.47 (12), p.1741-1748

2015

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Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids

Natural product reports, 2011-01, Vol.28 (7), p.1229-1260

2011

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Elements as Direct Feedstocks for Organic Synthesis: Fe/I 2 /O 2 for Diamination of 2-Cyclohexenones with 2-Aminopyrimidine and 2-Aminopyridines

Organic letters, 2015-10, Vol.17 (20), p.4956-4959

2015

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New Antimalarial and Antimicrobial Tryptamine Derivatives from the Marine Sponge Fascaplysinopsis reticulata

Marine drugs, 2019-03, Vol.17 (3), p.167

2019

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Isolation, Synthesis and Absolute Configuration of the Pericharaxins A and B, Epimeric Hydroxy-Polyene Glycerol Ethers from the Calcarean Sponge Pericharax heteroraphis

Marine drugs, 2022-10, Vol.20 (10), p.635

2022

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Quorum Sensing Inhibitory and Antifouling Activities of New Bromotyrosine Metabolites from the Polynesian Sponge Pseudoceratina n. sp

Marine drugs, 2020-05, Vol.18 (5), p.272

2020

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Chemistry and Biological Activities of the Marine Sponges of the Genera Mycale ( Arenochalina ), Biemna and Clathria

Marine drugs, 2018-06, Vol.16 (6), p.214

2018

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Chemical Diversity and Biological Activities of Marine Sponges of the Genus Suberea : A Systematic Review

Marine drugs, 2019-02, Vol.17 (2), p.115

2019

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Bioactive Bromotyrosine Derivatives from the Pacific Marine Sponge Suberea clavata (Pulitzer-Finali, 1982)

Marine drugs, 2021-03, Vol.19 (3), p.143

2021

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Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2‑Aminopyrimidine and 2‑Aminopyridines

Organic letters, 2016-05, Vol.18 (9), p.2177-2179

2016

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Unguiculin A and Ptilomycalins E–H, Antimalarial Guanidine Alkaloids from the Marine Sponge Monanchora unguiculata

Journal of natural products (Washington, D.C.), 2017-05, Vol.80 (5), p.1404-1410

2017

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Chemical Investigation of the Calcareous Marine Sponge Pericharax heteroraphis , Clathridine-A Related Derivatives Isolation, Synthesis and Osteogenic Activity

Marine drugs, 2024-04, Vol.22 (5), p.196

2024

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Cytotoxic Guanidine Alkaloids from a French Polynesian Monanchora n. sp. Sponge

Journal of natural products (Washington, D.C.), 2016-08, Vol.79 (8), p.1929-1937

2016

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Bioactive Bromotyrosine-Derived Alkaloids from the Polynesian Sponge Suberea ianthelliformis

Marine drugs, 2018-04, Vol.16 (5), p.146

2018

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Synergistic AML Cell Death Induction by Marine Cytotoxin (+)-1( R ), 6( S ), 1'( R ), 6'( S ), 11( R ), 17( S )-Fistularin-3 and Bcl-2 Inhibitor Venetoclax

Marine drugs, 2018-12, Vol.16 (12), p.518

2018

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Sponge's Molecular Diversity Through the Ambivalent Reactivity of 2-Aminoimidazole: A Universal Chemical Pathway to the Oroidin-Based Pyrrole-Imidazole Alkaloids and Their Palau'amine Congeners

European journal of organic chemistry, 2001-01, Vol.2001 (2), p.237-243

2001

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Selective autoxidation of benzylamines: application to the synthesis of some nitrogen heterocycles

Toward the Synthesis of Sceptrin and Benzosceptrin: Solvent Effect in Stereo‐ and Regioselective [2+2] Photodimerization and Easy Access to the Fully Substituted Benzobutane

Unaromatized Tetrahydrobenzimidazole Synthesis from p‐Benzoquinone and N‐Arylamidines and their Cytotoxic Potential

Short‐Cut Bio‐Inspired Synthesis of Tricyclic Guanidinic Motifs of Crambescidins and Batzelladines Marine Alkaloids

Tetrahydrobenzimidazole TMQ0153 triggers apoptosis, autophagy and necroptosis crosstalk in chronic myeloid leukemia

Elemental Sulfur Disproportionation in the Redox Condensation Reaction between o-Halonitrobenzenes and Benzylamines

Nitro-Methyl Redox Coupling: Efficient Approach to 2‑Hetarylbenzothiazoles from 2‑Halonitroarene, Methylhetarene, and Elemental Sulfur

Three-Component Reaction between Alkynes, Elemental Sulfur, and Aliphatic Amines: A General, Straightforward, and Atom Economical Approach to Thioamides

Benzazoles from Aliphatic Amines and o‑Amino/Mercaptan/Hydroxyanilines: Elemental Sulfur as a Highly Efficient and Traceless Oxidizing Agent

Sodium Sulfide: A Sustainable Solution for Unbalanced Redox Condensation Reaction between o-Nitroanilines and Alcohols Catalyzed by an Iron–Sulfur System

Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids

Elements as Direct Feedstocks for Organic Synthesis: Fe/I 2 /O 2 for Diamination of 2-Cyclohexenones with 2-Aminopyrimidine and 2-Aminopyridines

New Antimalarial and Antimicrobial Tryptamine Derivatives from the Marine Sponge Fascaplysinopsis reticulata

Isolation, Synthesis and Absolute Configuration of the Pericharaxins A and B, Epimeric Hydroxy-Polyene Glycerol Ethers from the Calcarean Sponge Pericharax heteroraphis

Quorum Sensing Inhibitory and Antifouling Activities of New Bromotyrosine Metabolites from the Polynesian Sponge Pseudoceratina n. sp

Chemistry and Biological Activities of the Marine Sponges of the Genera Mycale ( Arenochalina ), Biemna and Clathria

Chemical Diversity and Biological Activities of Marine Sponges of the Genus Suberea : A Systematic Review

Bioactive Bromotyrosine Derivatives from the Pacific Marine Sponge Suberea clavata (Pulitzer-Finali, 1982)

Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2‑Aminopyrimidine and 2‑Aminopyridines

Unguiculin A and Ptilomycalins E–H, Antimalarial Guanidine Alkaloids from the Marine Sponge Monanchora unguiculata

Chemical Investigation of the Calcareous Marine Sponge Pericharax heteroraphis , Clathridine-A Related Derivatives Isolation, Synthesis and Osteogenic Activity

Cytotoxic Guanidine Alkaloids from a French Polynesian Monanchora n. sp. Sponge

Bioactive Bromotyrosine-Derived Alkaloids from the Polynesian Sponge Suberea ianthelliformis

Synergistic AML Cell Death Induction by Marine Cytotoxin (+)-1( R ), 6( S ), 1'( R ), 6'( S ), 11( R ), 17( S )-Fistularin-3 and Bcl-2 Inhibitor Venetoclax

Sponge's Molecular Diversity Through the Ambivalent Reactivity of 2-Aminoimidazole: A Universal Chemical Pathway to the Oroidin-Based Pyrrole-Imidazole Alkaloids and Their Palau'amine Congeners

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