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Combining the Power of J Coupling and DP4 Analysis on Stereochemical Assignments: The J‑DP4 Methods

Organic letters, 2019-06, Vol.21 (11), p.4003-4007

2019

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Are Computational Methods Useful for Structure Elucidation of Large and Flexible Molecules? Belizentrin as a Case Study

Organic letters, 2021-01, Vol.23 (2), p.503-507

2021

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Dynamic Nucleophilic Aromatic Substitution of Tetrazines

Angewandte Chemie (International ed.), 2021-08, Vol.60 (34), p.18783-18791

International ed. in English, 2021

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May the Force (Field) Be with You: On the Importance of Conformational Searches in the Prediction of NMR Chemical Shifts

Marine drugs, 2022-11, Vol.20 (11), p.699

2022

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Chemical Stability of Petrichorins

Journal of organic chemistry, 2022-12, Vol.87 (24), p.16847-16850

2022

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Marine Microalgae: Promising Source for New Bioactive Compounds

Marine drugs, 2018-09, Vol.16 (9), p.317

2018

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Evaluation of Oxasqualenoids from the Red Alga Laurencia viridis against Acanthamoeba

Marine drugs, 2019-07, Vol.17 (7), p.420

2019

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Induction of New Aromatic Polyketides from the Marine Actinobacterium Streptomyces griseorubiginosus through an OSMAC Approach

Marine drugs, 2023-10, Vol.21 (10), p.526

2023

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Structure and Computational Basis for Backbone Rearrangement in Marine Oxasqualenoids

Journal of organic chemistry, 2021-02, Vol.86 (3), p.2437-2446

2021

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Connecting Discrete Stereoclusters by Using DFT and NMR Spectroscopy: The Case of Nivariol

Chemistry : a European journal, 2013-06, Vol.19 (26), p.8525-8532

2013

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Thermodynamics of Binding of d-Galactose and Deoxy Derivatives thereof to the l-Arabinose-binding Protein

Journal of the American Chemical Society, 2004-09, Vol.126 (38), p.11870-11876

2004

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Gongolarones as antiamoeboid chemical scaffold

Biomedicine & pharmacotherapy, 2023-02, Vol.158, p.114185-114185, Article 114185

2023

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On the Configuration of Five-Membered Rings: A Spin-Spin Coupling Constant Approach

Chemistry : a European journal, 2011-05, Vol.17 (23), p.6338-6347

2011

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Osteoprotective effect of the marine alkaloid norzoanthamine on an osteoporosis model in ovariectomized rat

Biomedicine & pharmacotherapy, 2022-03, Vol.147, p.112631-112631, Article 112631

2022

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Belizentrin, a Highly Bioactive Macrocycle from the Dinoflagellate Prorocentrum belizeanum

Organic letters, 2014-09, Vol.16 (17), p.4546-4549

2014

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OSMAC Approach and Cocultivation for the Induction of Secondary Metabolism of the Fungus Pleotrichocladium opacum

ACS omega, 2023-10, Vol.8 (42), p.39873-39885

2023

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Antiprotozoal activities of marine polyether triterpenoids

Bioorganic chemistry, 2019-11, Vol.92, p.103276, Article 103276

2019

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Pinnatifidenyne-Derived Ethynyl Oxirane Acetogenins from Laurencia viridis

Marine drugs, 2017-12, Vol.16 (1), p.5

2017

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Zoaramine, a Zoanthamine-like Alkaloid with a New Skeleton

Organic letters, 2014-06, Vol.16 (11), p.2880-2883

2014

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Polyoxygenated anti-inflammatory biscembranoids from the soft coral Sarcophyton tortuosum and their stereochemistry

Chinese chemical letters, 2021-01, Vol.32 (1), p.271-276

2021

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Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity

Marine drugs, 2018-04, Vol.16 (4), p.131

2018

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Oxasqualenoids from Laurencia viridis: Combined Spectroscopic–Computational Analysis and Antifouling Potential

Journal of natural products (Washington, D.C.), 2015-04, Vol.78 (4), p.712-721

2015

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New oxidized zoanthamines from a Canary Islands Zoanthus sp

Marine drugs, 2014-10, Vol.12 (10), p.5188-5196

2014

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Stereochemistry of complex marine natural products by quantum mechanical calculations of NMR chemical shifts: solvent and conformational effects on okadaic acid

Marine drugs, 2014-01, Vol.12 (1), p.176-192

2014

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Stereochemical determination of five-membered cyclic ether acetogenins using a spin-spin coupling constant approach and DFT calculations

Marine drugs, 2014-07, Vol.12 (7), p.4031-4044

2014

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Combining the Power of J Coupling and DP4 Analysis on Stereochemical Assignments: The J‑DP4 Methods

Are Computational Methods Useful for Structure Elucidation of Large and Flexible Molecules? Belizentrin as a Case Study

Dynamic Nucleophilic Aromatic Substitution of Tetrazines

May the Force (Field) Be with You: On the Importance of Conformational Searches in the Prediction of NMR Chemical Shifts

Chemical Stability of Petrichorins

Marine Microalgae: Promising Source for New Bioactive Compounds

Evaluation of Oxasqualenoids from the Red Alga Laurencia viridis against Acanthamoeba

Induction of New Aromatic Polyketides from the Marine Actinobacterium Streptomyces griseorubiginosus through an OSMAC Approach

Structure and Computational Basis for Backbone Rearrangement in Marine Oxasqualenoids

Connecting Discrete Stereoclusters by Using DFT and NMR Spectroscopy: The Case of Nivariol

Thermodynamics of Binding of d-Galactose and Deoxy Derivatives thereof to the l-Arabinose-binding Protein

Gongolarones as antiamoeboid chemical scaffold

On the Configuration of Five-Membered Rings: A Spin-Spin Coupling Constant Approach

Osteoprotective effect of the marine alkaloid norzoanthamine on an osteoporosis model in ovariectomized rat

Belizentrin, a Highly Bioactive Macrocycle from the Dinoflagellate Prorocentrum belizeanum

OSMAC Approach and Cocultivation for the Induction of Secondary Metabolism of the Fungus Pleotrichocladium opacum

Antiprotozoal activities of marine polyether triterpenoids

Pinnatifidenyne-Derived Ethynyl Oxirane Acetogenins from Laurencia viridis

Zoaramine, a Zoanthamine-like Alkaloid with a New Skeleton

Polyoxygenated anti-inflammatory biscembranoids from the soft coral Sarcophyton tortuosum and their stereochemistry

Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity

Oxasqualenoids from Laurencia viridis: Combined Spectroscopic–Computational Analysis and Antifouling Potential

New oxidized zoanthamines from a Canary Islands Zoanthus sp

Stereochemistry of complex marine natural products by quantum mechanical calculations of NMR chemical shifts: solvent and conformational effects on okadaic acid

Stereochemical determination of five-membered cyclic ether acetogenins using a spin-spin coupling constant approach and DFT calculations

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