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Italian chemists' contributions to named reactions in organic synthesis: an historical perspective

Molecules, 2013-09, Vol.18 (9), p.10870-10900

2013

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novel method based on click chemistry, which overcomes limitations of cell cycle analysis by classical determination of BrdU incorporation, allowing multiplex antibody staining

Cytometry. Part A, 2008-07, Vol.73A (7), p.626-636

2008

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From polymer to small organic molecules: a tight relationship between radical chemistry and solid-phase organic synthesis

Molecules (Basel, Switzerland), 2011-04, Vol.16 (4), p.3252-3314

2011

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Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining

Current Protocols in Cytometry, 2015-04, Vol.72 (1), p.7.34.1-7.34.17

2015

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Cover Feature: Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction (Chem. Eur. J. 50/2024)

Chemistry : a European journal, 2024-09, Vol.30 (50), p.n/a

2024

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Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction

Chemistry : a European journal, 2024-09, Vol.30 (50), p.e202402175-n/a

2024

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Pestalotiopsins A and B: New Caryophyllenes from an Endophytic Fungus of Taxus brevifolia

Journal of organic chemistry, 1996-03, Vol.61 (6), p.2122-2124

1996

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From “Click” to “Fenton” chemistry for 5‐bromo‐2′‐deoxyuridine determination

Cytometry. Part A, 2013-11, Vol.83 (11), p.989-1000

2013

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Traceless solid-phase synthesis of 2-amino-5-alkylidene-thiazol-4-ones

Tetrahedron letters, 2005-04, Vol.46 (14), p.2387-2391

2005

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Abstract 1615: NMS-812, a novel potent PERK inhibitor that also inhibits GCN2, exhibits strong anti-tumor activity as single agent and in combination in preclinical models

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.1615-1615

2023

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Application of Click Chemistry Conditions for 5‐Bromo‐2′‐Deoxyuridine Determination Through Fenton and Related Reactions

Current Protocols in Cytometry, 2015-01, Vol.71 (1), p.7.43.1-7.43.17

2015

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Abstract 5163: Characterization of NMS-E194, a selective and potent PERK inhibitor with efficacy in the KMS-11 multiple myeloma

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.5163-5163

2017

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3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 1. Lead Finding

Journal of medicinal chemistry, 2004-06, Vol.47 (13), p.3367-3380

2004

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Optimization of Diarylthiazole B-Raf Inhibitors: Identification of a Compound Endowed with High Oral Antitumor Activity, Mitigated hERG Inhibition, and Low Paradoxical Effect

ChemMedChem, 2015-02, Vol.10 (2), p.276-295

2015

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Thieno[3,2- c]pyrazoles: A novel class of Aurora inhibitors with favorable antitumor activity

Bioorganic & medicinal chemistry, 2010-10, Vol.18 (19), p.7113-7120

2010

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1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis

Tetrahedron, 2006-10, Vol.62 (43), p.10223-10236

2006

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Abstract 3754: Characterization of NMS-P285, a new highly selective and potent BRAF inhibitor

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.3754-3754

2012

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A cobalt-phosphine complex as mediator in the formation of carbon-carbon bonds

Journal of organic chemistry, 1994-01, Vol.59 (1), p.1-3

1994

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Amylase induction activity of fluorescein labeled gibberellin in barley aleurone protoplasts

Bioorganic & medicinal chemistry letters, 1996-11, Vol.6 (21), p.2549-2552

1996

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Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining

Current Protocols in Cytometry, 2008-07, Vol.45 (1), p.7.34.1-7.34.13

2008

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Abstract 2522: Identification and characterization of new highly selective and potent BRAF inhibitors

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.2522-2522

2010

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Trifluoroacetic Anhydride-Mediated Solid-Phase Version of the Robinson−Gabriel Synthesis of Oxazoles

Journal of combinatorial chemistry, 2005-05, Vol.7 (3), p.463-473

2005

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Metabolites of Pestalotiopsis spp., endophytic fungi of Taxus brevifolia

Phytochemistry (Oxford), 1997-09, Vol.46 (2), p.313-319

1997

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ChemInform Abstract: From Polymer to Small Organic Molecules: A Tight Relationship Between Radical Chemistry and Solid-Phase Organic Synthesis

ChemInform, 2011-09, Vol.42 (36), p.no-no

2011

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A New Isodrimeninol from Pestalotiopsis sp

Journal of natural products (Washington, D.C.), 1996-01, Vol.59 (1), p.47-48

1996

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Italian chemists' contributions to named reactions in organic synthesis: an historical perspective

novel method based on click chemistry, which overcomes limitations of cell cycle analysis by classical determination of BrdU incorporation, allowing multiplex antibody staining

From polymer to small organic molecules: a tight relationship between radical chemistry and solid-phase organic synthesis

Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining

Cover Feature: Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction (Chem. Eur. J. 50/2024)

Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction

Pestalotiopsins A and B: New Caryophyllenes from an Endophytic Fungus of Taxus brevifolia

From “Click” to “Fenton” chemistry for 5‐bromo‐2′‐deoxyuridine determination

Traceless solid-phase synthesis of 2-amino-5-alkylidene-thiazol-4-ones

Abstract 1615: NMS-812, a novel potent PERK inhibitor that also inhibits GCN2, exhibits strong anti-tumor activity as single agent and in combination in preclinical models

Application of Click Chemistry Conditions for 5‐Bromo‐2′‐Deoxyuridine Determination Through Fenton and Related Reactions

Abstract 5163: Characterization of NMS-E194, a selective and potent PERK inhibitor with efficacy in the KMS-11 multiple myeloma

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 1. Lead Finding

Optimization of Diarylthiazole B-Raf Inhibitors: Identification of a Compound Endowed with High Oral Antitumor Activity, Mitigated hERG Inhibition, and Low Paradoxical Effect

Thieno[3,2- c]pyrazoles: A novel class of Aurora inhibitors with favorable antitumor activity

1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis

Abstract 3754: Characterization of NMS-P285, a new highly selective and potent BRAF inhibitor

A cobalt-phosphine complex as mediator in the formation of carbon-carbon bonds

Amylase induction activity of fluorescein labeled gibberellin in barley aleurone protoplasts

Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining

Abstract 2522: Identification and characterization of new highly selective and potent BRAF inhibitors

Trifluoroacetic Anhydride-Mediated Solid-Phase Version of the Robinson−Gabriel Synthesis of Oxazoles

Metabolites of Pestalotiopsis spp., endophytic fungi of Taxus brevifolia

ChemInform Abstract: From Polymer to Small Organic Molecules: A Tight Relationship Between Radical Chemistry and Solid-Phase Organic Synthesis

A New Isodrimeninol from Pestalotiopsis sp

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