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An efficient synthesis of 1-arylindazole-3-carboxamides using nitrile imines, isocyanides and 2-hydroxymethylbenzoic acid, followed by a chemoselective Buchwald–Hartwig intramolecular cyclization

RSC advances, 2016-01, Vol.6 (41), p.34913-34920

2016

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Role of the nicotinic acid group in NAADP receptor selectivity

Cell calcium (Edinburgh), 2005, Vol.37 (1), p.81-86

2005

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Ingenol derivatives inhibit proliferation and induce apoptosis in breast cancer cell lines

European journal of gynaecological oncology, 2005, Vol.26 (5), p.526-530

2005

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Efficient Synthesis of α-Ketoamides via 2-Acyl-5-aminooxazoles by Reacting Acyl Chlorides and α-Isocyanoacetamides

Organic letters, 2010-02, Vol.12 (4), p.820-823

2010

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Unnatural Natural Products from the Transannular Cyclization of Lathyrane Diterpenes

Organic letters, 2001-05, Vol.3 (11), p.1609-1612

2001

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Synthesis of NO-Donor Bisphosphonates and Their in-Vitro Action on Bone Resorption

Journal of medicinal chemistry, 2005-03, Vol.48 (5), p.1322-1329

2005

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Macrocyclic diterpenoids from Euphorbia semiperfoliata

Journal of natural products (Washington, D.C.), 1998-06, Vol.61 (6), p.749-756

1998

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Diterpenoids from Euphorbia pithyusa subsp. cupanii

Journal of natural products (Washington, D.C.), 1999-10, Vol.62 (10), p.1399-1404

1999

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An expeditious procedure for the isolation of ingenol from the seeds of Euphorbia lathyris

Journal of natural products (Washington, D.C.), 1999-01, Vol.62 (1), p.76-79

1999

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Medicinal Chemistry of Combretastatin A4: Present and Future Directions

Journal of medicinal chemistry, 2006-06, Vol.49 (11), p.3033-3044

2006

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Rapid Synthesis of Triazole-Modified Resveratrol Analogues via Click Chemistry

Journal of medicinal chemistry, 2006-01, Vol.49 (2), p.467-470

2006

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An efficient synthesis of 1-arylindazole-3-carboxamides using nitrile imines, isocyanides and 2-hydroxymethylbenzoic acid, followed by a chemoselective Buchwald-Hartwig intramolecular cyclizationElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ra01442a

2016-04

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ChemInform Abstract: An Efficient Synthesis of 1‐Arylindazole‐3‐carboxamides Using Nitrile Imines, Isocyanides and 2‐Hydroxymethylbenzoic Acid, Followed by a Chemoselective Buchwald—Hartwig Intramolecular Cyclization

ChemInform, 2016-08, Vol.47 (34), p.no-no

2016

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Identification of a novel NAMPT inhibitor by combinatorial click chemistry and chemical refinement

MedChemComm, 2015, Vol.6 (10), p.1891-1897

2015

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Identification of a novel NAMPT inhibitor by combinatorial click chemistry and chemical refinementElectronic supplementary information (ESI) available: Materials and methods. See DOI: 10.1039/c5md00261c

2015-10

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Synthesis and Cytotoxic Evaluation of Combretafurazans

Journal of medicinal chemistry, 2005-05, Vol.48 (9), p.3260-3268

2005

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A Mimicry of Primary Amines by Bis-Secondary Diamines as Components in the Ugi Four-Component Reaction

Angewandte Chemie (International ed.), 2006-02, Vol.45 (7), p.1099-1102

2006

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Chemoselective Esterification of Phenolic Acids and Alcohols

Organic letters, 2002-10, Vol.4 (22), p.3839-3841

2002

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Macrocyclic diterpenoids from Euphorbia semiperfoliata

Journal of natural products (Washington, D.C.), 1998-06, Vol.61 (6), p.749-756

1998

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A Three-Component Synthesis of (1,3-Oxazol-2-yl)-1,2-dihydro(iso)quinoline and its further Structural Diversifications

Synlett, 2005-02, Vol.2005 (3), p.532-534

2005

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Polycyclic diterpenoids from Euphorbia characias

Fitoterapia, 2000-04, Vol.71 (2), p.134-142

2000

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Synthesis and biological activity of mustard derivatives of combretastatins

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (15), p.3551-3554

2005

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Bisnorsesquiterpenoids from Euphorbia resinifera Berg. and an Expeditious Procedure to Obtain Resiniferatoxin from Its Fresh Latex

European journal of organic chemistry, 2002-01, Vol.2002 (1), p.71-78

2002

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Development of a new class of potential antiatherosclerosis agents: NO-donor antioxidants

Bioorganic & medicinal chemistry letters, 2004-12, Vol.14 (24), p.5971-5974

2004

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An efficient synthesis of 1-arylindazole-3-carboxamides using nitrile imines, isocyanides and 2-hydroxymethylbenzoic acid, followed by a chemoselective Buchwald–Hartwig intramolecular cyclization

Role of the nicotinic acid group in NAADP receptor selectivity

Ingenol derivatives inhibit proliferation and induce apoptosis in breast cancer cell lines

Efficient Synthesis of α-Ketoamides via 2-Acyl-5-aminooxazoles by Reacting Acyl Chlorides and α-Isocyanoacetamides

Unnatural Natural Products from the Transannular Cyclization of Lathyrane Diterpenes

Synthesis of NO-Donor Bisphosphonates and Their in-Vitro Action on Bone Resorption

Macrocyclic diterpenoids from Euphorbia semiperfoliata

Diterpenoids from Euphorbia pithyusa subsp. cupanii

An expeditious procedure for the isolation of ingenol from the seeds of Euphorbia lathyris

Medicinal Chemistry of Combretastatin A4: Present and Future Directions

Rapid Synthesis of Triazole-Modified Resveratrol Analogues via Click Chemistry

An efficient synthesis of 1-arylindazole-3-carboxamides using nitrile imines, isocyanides and 2-hydroxymethylbenzoic acid, followed by a chemoselective Buchwald-Hartwig intramolecular cyclizationElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ra01442a

ChemInform Abstract: An Efficient Synthesis of 1‐Arylindazole‐3‐carboxamides Using Nitrile Imines, Isocyanides and 2‐Hydroxymethylbenzoic Acid, Followed by a Chemoselective Buchwald—Hartwig Intramolecular Cyclization

Identification of a novel NAMPT inhibitor by combinatorial click chemistry and chemical refinement

Identification of a novel NAMPT inhibitor by combinatorial click chemistry and chemical refinementElectronic supplementary information (ESI) available: Materials and methods. See DOI: 10.1039/c5md00261c

Synthesis and Cytotoxic Evaluation of Combretafurazans

A Mimicry of Primary Amines by Bis-Secondary Diamines as Components in the Ugi Four-Component Reaction

Chemoselective Esterification of Phenolic Acids and Alcohols

Macrocyclic diterpenoids from Euphorbia semiperfoliata

A Three-Component Synthesis of (1,3-Oxazol-2-yl)-1,2-dihydro(iso)quinoline and its further Structural Diversifications

Polycyclic diterpenoids from Euphorbia characias

Synthesis and biological activity of mustard derivatives of combretastatins

Bisnorsesquiterpenoids from Euphorbia resinifera Berg. and an Expeditious Procedure to Obtain Resiniferatoxin from Its Fresh Latex

Development of a new class of potential antiatherosclerosis agents: NO-donor antioxidants

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