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A small-molecule inhibitor of BamA impervious to efflux and the outer membrane permeability barrier

Proceedings of the National Academy of Sciences - PNAS, 2019-10, Vol.116 (43), p.21748-21757

2019

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Efforts toward Expansion of the Genetic Alphabet: DNA Polymerase Recognition of a Highly Stable, Self-Pairing Hydrophobic Base

Journal of the American Chemical Society, 1999-12, Vol.121 (49), p.11585-11586

1999

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Efforts toward Expansion of the Genetic Alphabet: Optimization of Interbase Hydrophobic Interactions

Journal of the American Chemical Society, 2000-08, Vol.122 (32), p.7621-7632

2000

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Discovery of novel non-steroidal reverse indole mineralocorticoid receptor antagonists

Bioorganic & medicinal chemistry letters, 2016-06, Vol.26 (12), p.2866-2869

2016

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A Model for Binding of Structurally Diverse Natural Product Inhibitors of Protein Phosphatases PP1 and PP2A

Journal of medicinal chemistry, 1997-09, Vol.40 (20), p.3199-3206

1997

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Efforts toward the Expansion of the Genetic Alphabet: Information Storage and Replication with Unnatural Hydrophobic Base Pairs

Journal of the American Chemical Society, 2000-04, Vol.122 (14), p.3274-3287

2000

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Glucose-lowering in a db/db mouse model by dihydropyridine diacid glycogen phosphorylase inhibitors

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (20), p.3405-3408

2003

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A Phototautomerizable Model DNA Base Pair

Journal of the American Chemical Society, 2000-10, Vol.122 (41), p.9917-9920

2000

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Universal bases for hybridization, replication and chain termination

Nucleic acids research, 2000-08, Vol.28 (15), p.2911-2914

2000

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Novel 3,4-dihydroquinolin-2(1H)-one inhibitors of human glycogen phosphorylase a

Bioorganic & medicinal chemistry letters, 2003-12, Vol.13 (24), p.4385-4388

2003

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Rational Design of an Unnatural Base Pair with Increased Kinetic Selectivity

Journal of the American Chemical Society, 2000-09, Vol.122 (36), p.8803-8804

2000

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Total Synthesis of Calyculin C

Journal of the American Chemical Society, 1998-12, Vol.120 (48), p.12435-12442

1998

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Chemically Reactive Immunogens Lead to Functional Convergence of the Immune Response

Journal of the American Chemical Society, 2000-11, Vol.122 (44), p.10743-10753

2000

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Asymmetric Synthesis of Calyculin C. 1. Synthesis of the C1−C25 Fragment

Journal of organic chemistry, 1996-09, Vol.61 (18), p.6139-6152

1996

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Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C26−C37 Fragment and Model Wittig Couplings

Journal of organic chemistry, 1996-09, Vol.61 (18), p.6153-6161

1996

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Stable and Selective Hybridization of Oligonucleotides with Unnatural Hydrophobic Bases

Angewandte Chemie (International ed.), 2000-08, Vol.39 (16), p.2940-2942

2000

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Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C(26)-C(37) Fragment and Model Wittig Couplings

Journal of organic chemistry, 1996-09, Vol.61 (18), p.6153-6161

1996

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Asymmetric Synthesis of Calyculin C. 1. Synthesis of the C(1)-C(25) Fragment

Journal of organic chemistry, 1996-09, Vol.61 (18), p.6139-6152

1996

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Asymmetric Synthesis of Calyculin C. 1. Synthesis of the C 1 −C 25 Fragment

Journal of organic chemistry, 1996-09, Vol.61 (18), p.6139-6152

1996

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Stabile und selektive Hybridisierung von Oligonucleotiden unter Verwendung nichtnatürlicher hydrophober Basen

Angewandte Chemie, 2000-08, Vol.112 (16), p.3069-3071

2000

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Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C 26 −C 37 Fragment and Model Wittig Couplings

Journal of organic chemistry, 1996-09, Vol.61 (18), p.6153-6161

1996

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Stabile und selektive Hybridisierung von Oligonucleotiden unter Verwendung nichtnatürlicher hydrophober Basen

Angewandte Chemie, 2000-08, Vol.112 (16), p.3069-3071

2000

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ChemInform Abstract: Total Synthesis of Calyculin C

ChemInform, 1999-04, Vol.30 (17), p.no-no

1999

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Novel 3,4-Dihydroquinolin-2(1H)-one Inhibitors of Human Glycogen Phosphorylase a

ChemInform, 2004-04, Vol.35 (14), p.no-no

2004

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Glucose-Lowering in a db/db Mouse Model by Dihydropyridine Diacid Glycogen Phosphorylase Inhibitors

ChemInform, 2004-01, Vol.35 (3), p.no-no

2004

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A small-molecule inhibitor of BamA impervious to efflux and the outer membrane permeability barrier

Efforts toward Expansion of the Genetic Alphabet: DNA Polymerase Recognition of a Highly Stable, Self-Pairing Hydrophobic Base

Efforts toward Expansion of the Genetic Alphabet: Optimization of Interbase Hydrophobic Interactions

Discovery of novel non-steroidal reverse indole mineralocorticoid receptor antagonists

A Model for Binding of Structurally Diverse Natural Product Inhibitors of Protein Phosphatases PP1 and PP2A

Efforts toward the Expansion of the Genetic Alphabet: Information Storage and Replication with Unnatural Hydrophobic Base Pairs

Glucose-lowering in a db/db mouse model by dihydropyridine diacid glycogen phosphorylase inhibitors

A Phototautomerizable Model DNA Base Pair

Universal bases for hybridization, replication and chain termination

Novel 3,4-dihydroquinolin-2(1H)-one inhibitors of human glycogen phosphorylase a

Rational Design of an Unnatural Base Pair with Increased Kinetic Selectivity

Total Synthesis of Calyculin C

Chemically Reactive Immunogens Lead to Functional Convergence of the Immune Response

Asymmetric Synthesis of Calyculin C. 1. Synthesis of the C1−C25 Fragment

Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C26−C37 Fragment and Model Wittig Couplings

Stable and Selective Hybridization of Oligonucleotides with Unnatural Hydrophobic Bases

Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C(26)-C(37) Fragment and Model Wittig Couplings

Asymmetric Synthesis of Calyculin C. 1. Synthesis of the C(1)-C(25) Fragment

Asymmetric Synthesis of Calyculin C. 1. Synthesis of the C 1 −C 25 Fragment

Stabile und selektive Hybridisierung von Oligonucleotiden unter Verwendung nichtnatürlicher hydrophober Basen

Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C 26 −C 37 Fragment and Model Wittig Couplings

Stabile und selektive Hybridisierung von Oligonucleotiden unter Verwendung nichtnatürlicher hydrophober Basen

ChemInform Abstract: Total Synthesis of Calyculin C

Novel 3,4-Dihydroquinolin-2(1H)-one Inhibitors of Human Glycogen Phosphorylase a

Glucose-Lowering in a db/db Mouse Model by Dihydropyridine Diacid Glycogen Phosphorylase Inhibitors

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