UB Paderborn / Katalog / Suche / in CDI

Charting Biologically Relevant Spirocyclic Compound Space

Chemistry : a European journal, 2017-01, Vol.23 (3), p.703-710

2017

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Fast Iterative Synthetic Approach toward Identification of Novel Highly Selective p38 MAP Kinase Inhibitors

Journal of medicinal chemistry, 2019-12, Vol.62 (23), p.10757-10782

2019

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Expansion of chemical space for collaborative lead generation and drug discovery: the European Lead Factory Perspective

Drug discovery today, 2015-11, Vol.20 (11), p.1310-1316

2015

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Rapid and Scalable Access into Strained Scaffolds through Continuous Flow Photochemistry

Organic process research & development, 2016-02, Vol.20 (2), p.409-413

2016

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Microwave-assisted diastereoselective two-step three-component synthesis for rapid access to drug-like libraries of substituted 3-amino-β-lactams

Bioorganic & medicinal chemistry, 2018-01, Vol.26 (1), p.41-49

2018

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Piperidine and octahydropyrano[3,4-c] pyridine scaffolds for drug-like molecular libraries of the European Lead Factory

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (19), p.5160-5170

2017

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Cyclopentitol as a scaffold for a natural product-like compound library for drug discovery

Bioorganic & medicinal chemistry, 2015-06, Vol.23 (11), p.2650-2655

2015

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Synthesis of the Right-Hand Substructure of Solanoeclepin A

European journal of organic chemistry, 2001-06, Vol.2001 (12), p.2371-2377

2001

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Intramolecular Photochemical Dioxenone−Alkene [2 + 2] Cycloadditions as an Approach to the Bicyclo[2.1.1]hexane Moiety of Solanoeclepin A

Journal of organic chemistry, 2001-01, Vol.66 (1), p.233-242

2001

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IMI European Lead Factory - democratizing access to high-throughput screening

Nature reviews. Drug discovery, 2022-04, Vol.21 (4), p.245-246

2022

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Studies towards the total synthesis of solanoeclepin A: synthesis of the 7-oxabicyclo[2.2.1]heptane moiety and attempted seven-membered ring formation

Perkin 1 : an international journal of organic and bio-organic chemistry, 2002-07 (14), p.1693-1700

2002

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Intramolecular [2+2] photocycloadditions as an approach towards the right-hand side of solanoeclepin A

Perkin 1 : an international journal of organic and bio-organic chemistry, 2001 (18), p.2250-2256

2001

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Synthesis of reduced collagen crosslinks

Bioorganic & medicinal chemistry letters, 1999-06, Vol.9 (12), p.1673-1676

1999

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Intramolecular [2+2] photocycloadditions as an approach towards the bicyclo[2.1.1]hexane substructure of solanoeclepin A

Chemical communications (Cambridge, England), 2000-01 (16), p.1463-1464

2000

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Studies towards the total synthesis of solanoeclepin A: synthesis and potato cyst nematode hatching activity of analogues containing the tetracyclic left-hand substructureElectronic supplementary information (ESI) available: further experimental details. See http://www.rsc.org/suppdata/p1/b2/b202020n

Perkin 1 : an international journal of organic and bio-organic chemistry, 2002-07 (14), p.1701-1713

2002

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Enantioselective synthesis of the tetracyclic left-hand substructure of solanoeclepin A

Chemical communications (Cambridge, England), 2000 (16), p.1465-1466

2000

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ChemInform Abstract: Intramolecular [2 + 2] Photocycloadditions as an Approach Towards the Right-Hand Side of Solanoeclepin A

ChemInform, 2002-02, Vol.33 (8), p.no-no

2002

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Studies Towards the Total Synthesis of Solanoeclepin A: Synthesis of the 7-Oxabicyclo[2.2.1]heptane Moiety and Attempted Seven-Membered Ring Formation

ChemInform, 2002-11, Vol.33 (47), p.202-202

2002

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ChemInform Abstract: Synthesis of the Right-Hand Substructure (I) of Solanoeclepin A

ChemInform, 2002-03, Vol.33 (11), p.no-no

2002

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Studies Towards the Total Synthesis of Solanoeclepin A: Synthesis and Potato Cyst Nematode Hatching Activity of Analogues Containing the Tetracyclic Left-Hand Substructure

ChemInform, 2002-11, Vol.33 (47), p.203-203

2002

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ChemInform Abstract: Enantioselective Synthesis of the Tetracyclic Left-Hand Substructure of Solanoeclepin A

ChemInform, 2000-12, Vol.31 (49), p.no-no

2000

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ChemInform Abstract: Synthesis of Reduced Collagen Crosslinks

ChemInform, 1999-09, Vol.30 (36), p.no-no

1999

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ChemInform Abstract: Intramolecular Photochemical Dioxenone-Alkene [2 + 2] Cycloadditions as an Approach to the Bicyclo[2.1.1]hexane Moiety of Solanoeclepin A

ChemInform, 2001-06, Vol.32 (25), p.no-no

2001

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ChemInform Abstract: Intramolecular [2 + 2] Photocycloadditions as an Approach Towards the Bicyclo[2.1.1]hexane Substructure of Solanoeclepin A

ChemInform, 2000-12, Vol.31 (49), p.no-no

2000

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Charting Biologically Relevant Spirocyclic Compound Space

Fast Iterative Synthetic Approach toward Identification of Novel Highly Selective p38 MAP Kinase Inhibitors

Expansion of chemical space for collaborative lead generation and drug discovery: the European Lead Factory Perspective

Rapid and Scalable Access into Strained Scaffolds through Continuous Flow Photochemistry

Microwave-assisted diastereoselective two-step three-component synthesis for rapid access to drug-like libraries of substituted 3-amino-β-lactams

Piperidine and octahydropyrano[3,4-c] pyridine scaffolds for drug-like molecular libraries of the European Lead Factory

Cyclopentitol as a scaffold for a natural product-like compound library for drug discovery

Synthesis of the Right-Hand Substructure of Solanoeclepin A

Intramolecular Photochemical Dioxenone−Alkene [2 + 2] Cycloadditions as an Approach to the Bicyclo[2.1.1]hexane Moiety of Solanoeclepin A

IMI European Lead Factory - democratizing access to high-throughput screening

Studies towards the total synthesis of solanoeclepin A: synthesis of the 7-oxabicyclo[2.2.1]heptane moiety and attempted seven-membered ring formation

Intramolecular [2+2] photocycloadditions as an approach towards the right-hand side of solanoeclepin A

Synthesis of reduced collagen crosslinks

Intramolecular [2+2] photocycloadditions as an approach towards the bicyclo[2.1.1]hexane substructure of solanoeclepin A

Enantioselective synthesis of the tetracyclic left-hand substructure of solanoeclepin A

ChemInform Abstract: Intramolecular [2 + 2] Photocycloadditions as an Approach Towards the Right-Hand Side of Solanoeclepin A

Studies Towards the Total Synthesis of Solanoeclepin A: Synthesis of the 7-Oxabicyclo[2.2.1]heptane Moiety and Attempted Seven-Membered Ring Formation

ChemInform Abstract: Synthesis of the Right-Hand Substructure (I) of Solanoeclepin A

Studies Towards the Total Synthesis of Solanoeclepin A: Synthesis and Potato Cyst Nematode Hatching Activity of Analogues Containing the Tetracyclic Left-Hand Substructure

ChemInform Abstract: Enantioselective Synthesis of the Tetracyclic Left-Hand Substructure of Solanoeclepin A

ChemInform Abstract: Synthesis of Reduced Collagen Crosslinks

ChemInform Abstract: Intramolecular Photochemical Dioxenone-Alkene [2 + 2] Cycloadditions as an Approach to the Bicyclo[2.1.1]hexane Moiety of Solanoeclepin A

ChemInform Abstract: Intramolecular [2 + 2] Photocycloadditions as an Approach Towards the Bicyclo[2.1.1]hexane Substructure of Solanoeclepin A

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