UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

(Invited) Development Status of EUV Resist toward Sub-20nmhp

ECS transactions, 2013, Vol.52 (1), p.245-250

Kimura, Tooru

2013

Volltextzugriff (PDF)

Novel and efficient synthesis of difficult sequence-containing peptides through O-N intramolecular acyl migration reaction of O-acyl isopeptides

Chemical communications (Cambridge, England), 2004 (1), p.124-125

2004

Volltextzugriff (PDF)

Structure of HIV-1 protease in complex with potent inhibitor KNI-272 determined by high-resolution X-ray and neutron crystallography

Proceedings of the National Academy of Sciences - PNAS, 2009-03, Vol.106 (12), p.4641-4646

2009

Volltextzugriff (PDF)

Development of O-acyl isopeptide method

Biopolymers, 2007, Vol.88 (2), p.253-262

2007

Volltextzugriff (PDF)

"Click Peptide": pH-Triggered in Situ Production and Aggregation of Monomer Aβ1-42

Chembiochem : a European journal of chemical biology, 2009-03, Vol.10 (4), p.710-715

2009

Volltextzugriff (PDF)

Design and synthesis of a novel water-soluble Aβ1-42 isopeptide: an efficient strategy for the preparation of Alzheimer's disease-related peptide, Aβ1-42, via O– N intramolecular acyl migration reaction

Tetrahedron letters, 2004-07, Vol.45 (31), p.5965-5968

2004

Volltextzugriff (PDF)

Development of first photoresponsive prodrug of paclitaxel

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (17), p.4492-4496

2006

Volltextzugriff (PDF)

Development of EUV Resist for 16nm Half Pitch

Journal of Photopolymer Science and Technology, 2012/06/26, Vol.25(5), pp.603-607

2012

Volltextzugriff (PDF)

Design of Potent Aspartic Protease Inhibitors to Treat Various Diseases

Archiv der Pharmazie (Weinheim), 2008-09, Vol.341 (9), p.523-535

2008

Volltextzugriff (PDF)

High-Affinity Inhibition of a Family of Plasmodium falciparum Proteases by a Designed Adaptive Inhibitor

Biochemistry (Easton), 2003-07, Vol.42 (28), p.8459-8464

2003

Volltextzugriff (PDF)

O-acyl isopeptide method: efficient synthesis of isopeptide segment and application to racemization-free segment condensation

Organic & biomolecular chemistry, 2009-01, Vol.7 (14), p.2894

2009

Volltextzugriff (PDF)

The 'O-acyl isopeptide method' for the synthesis of difficult sequence-containing peptides: application to the synthesis of Alzheimer's disease-related amyloid β peptide (Aβ) 1-42

Journal of peptide science, 2005-08, Vol.11 (8), p.441-451

2005

Volltextzugriff (PDF)

Combination of Non-natural d-Amino Acid Derivatives and Allophenylnorstatine−Dimethylthioproline Scaffold in HIV Protease Inhibitors Have High Efficacy in Mutant HIV

Journal of medicinal chemistry, 2008-05, Vol.51 (10), p.2992-3004

2008

Volltextzugriff (PDF)

‘ O-Acyl isopeptide method’ for the efficient synthesis of difficult sequence-containing peptides: use of ‘ O-acyl isodipeptide unit’

Tetrahedron letters, 2006-05, Vol.47 (18), p.3013-3017

2006

Volltextzugriff (PDF)

Inhibitory effect of a dimerization-arm-mimetic peptide on EGF receptor activation

Bioorganic & medicinal chemistry letters, 2009-06, Vol.19 (12), p.3279-3282

2009

Volltextzugriff (PDF)

Antimalarial activity enhancement in hydroxymethylcarbonyl (HMC) isostere-based dipeptidomimetics targeting malarial aspartic protease plasmepsin

Bioorganic & medicinal chemistry, 2008-12, Vol.16 (23), p.10049-10060

2008

Volltextzugriff (PDF)

Identification and Characterization of Allophenylnorstatine-Based Inhibitors of Plasmepsin II, an Antimalarial Target

Biochemistry (Easton), 2002-02, Vol.41 (7), p.2273-2280

2002

Volltextzugriff (PDF)

Novel Material Development for EUV Resist towards sub-20nm half pitch

Journal of Photopolymer Science and Technology, 2011/06/21, Vol.24(2), pp.199-204

2011

Volltextzugriff (PDF)

Improvement of both plasmepsin inhibitory activity and antimalarial activity by 2-aminoethylamino substitution

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4836-4839

2010

Volltextzugriff (PDF)

Maintaining potent HTLV-I protease inhibition without the P3-cap moiety in small tetrapeptidic inhibitors

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (6), p.1832-1837

2011

Volltextzugriff (PDF)

Small-Sized Human Immunodeficiency Virus Type-1 Protease Inhibitors Containing Allophenylnorstatine to Explore the S2′ Pocket

Journal of medicinal chemistry, 2009-12, Vol.52 (23), p.7604-7617

2009

Volltextzugriff (PDF)

Structural Changes of Photoresist on Wafer Studied by Pyrolysis-GC/MS Combined with Micro-GPC

Journal of Photopolymer Science and Technology, 2014/07/08, Vol.27(1), pp.41-48

2014

Volltextzugriff (PDF)

Epimerization-free synthesis of cyclic peptide by use of the O-acyl isopeptide method

Journal of peptide science, 2010-08, Vol.16 (8), p.437-442

2010

Volltextzugriff (PDF)

ON intramolecular acyl migration reaction in the development of prodrugs and the synthesis of difficult sequence-containing bioactive peptides

Biopolymers, 2004, Vol.76 (4), p.344-356

2004

Volltextzugriff (PDF)

Locking the two ends of tetrapeptidic HTLV-I protease inhibitors inside the enzyme

Bioorganic & medicinal chemistry, 2008-07, Vol.16 (14), p.6880-6890

2008

Volltextzugriff (PDF)

1 – 25 von 391

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(298)
Mit Volltextzugriff
(345)

Publikationsform

Sprache

Englisch
(358)
Japanisch
(172)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

(Invited) Development Status of EUV Resist toward Sub-20nmhp

Novel and efficient synthesis of difficult sequence-containing peptides through O-N intramolecular acyl migration reaction of O-acyl isopeptides

Structure of HIV-1 protease in complex with potent inhibitor KNI-272 determined by high-resolution X-ray and neutron crystallography

Development of O-acyl isopeptide method

"Click Peptide": pH-Triggered in Situ Production and Aggregation of Monomer Aβ1-42

Design and synthesis of a novel water-soluble Aβ1-42 isopeptide: an efficient strategy for the preparation of Alzheimer's disease-related peptide, Aβ1-42, via O– N intramolecular acyl migration reaction

Development of first photoresponsive prodrug of paclitaxel

Development of EUV Resist for 16nm Half Pitch

Design of Potent Aspartic Protease Inhibitors to Treat Various Diseases

High-Affinity Inhibition of a Family of Plasmodium falciparum Proteases by a Designed Adaptive Inhibitor

O-acyl isopeptide method: efficient synthesis of isopeptide segment and application to racemization-free segment condensation

The 'O-acyl isopeptide method' for the synthesis of difficult sequence-containing peptides: application to the synthesis of Alzheimer's disease-related amyloid β peptide (Aβ) 1-42

Combination of Non-natural d-Amino Acid Derivatives and Allophenylnorstatine−Dimethylthioproline Scaffold in HIV Protease Inhibitors Have High Efficacy in Mutant HIV

‘ O-Acyl isopeptide method’ for the efficient synthesis of difficult sequence-containing peptides: use of ‘ O-acyl isodipeptide unit’

Inhibitory effect of a dimerization-arm-mimetic peptide on EGF receptor activation

Antimalarial activity enhancement in hydroxymethylcarbonyl (HMC) isostere-based dipeptidomimetics targeting malarial aspartic protease plasmepsin

Identification and Characterization of Allophenylnorstatine-Based Inhibitors of Plasmepsin II, an Antimalarial Target

Novel Material Development for EUV Resist towards sub-20nm half pitch

Improvement of both plasmepsin inhibitory activity and antimalarial activity by 2-aminoethylamino substitution

Maintaining potent HTLV-I protease inhibition without the P3-cap moiety in small tetrapeptidic inhibitors

Small-Sized Human Immunodeficiency Virus Type-1 Protease Inhibitors Containing Allophenylnorstatine to Explore the S2′ Pocket

Structural Changes of Photoresist on Wafer Studied by Pyrolysis-GC/MS Combined with Micro-GPC

Epimerization-free synthesis of cyclic peptide by use of the O-acyl isopeptide method

ON intramolecular acyl migration reaction in the development of prodrugs and the synthesis of difficult sequence-containing bioactive peptides

Locking the two ends of tetrapeptidic HTLV-I protease inhibitors inside the enzyme

Suchergebnisse filtern