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Novel riboswitch-binding flavin analog that protects mice against Clostridium difficile infection without inhibiting cecal flora

Antimicrobial agents and chemotherapy, 2015-09, Vol.59 (9), p.5736-5746

2015

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Continuous Flow Homolytic Aromatic Substitution with Electrophilic Radicals: A Fast and Scalable Protocol for Trifluoromethylation

Chemistry : a European journal, 2017-01, Vol.23 (1), p.176-186

2017

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Greene's Protective Groups in Organic Synthesis

Wuts, Peter G. M

Fifth edition., 2014

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Greene's Protective Groups in Organic Synthesis

4. Aufl., 2006

Volltextzugriff (PDF)

Greene’s protective groups in organic synthesis, fifth edition

Wuts, Peter G. M

5th ed., 2014

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Generation of Broad-Spectrum Antifungal Drug Candidates from the Natural Product Compound Aureobasidin A

ACS medicinal chemistry letters, 2015-06, Vol.6 (6), p.645-649

2015

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The Synthesis of Oxazolines Using the Vilsmeier Reagent

Journal of organic chemistry, 2000-12, Vol.65 (26), p.9223-9225

2000

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New Process for the Preparation of Methyl Carbonates

Organic letters, 2003-05, Vol.5 (9), p.1483-1485

2003

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A Practical Synthesis of Cabergoline

Journal of organic chemistry, 2002-10, Vol.67 (20), p.7147-7150

2002

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Development of a practical synthesis of sumanirole

Pure and applied chemistry, 2002-01, Vol.74 (8), p.1359-1368

2002

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A Scalable Synthesis of the INOS Inhibitor PHA-399733

Organic process research & development, 2009-03, Vol.13 (2), p.331-335

2009

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The addition of .gamma.-(trimethylsilyl)allylboronates to imines

Journal of organic chemistry, 1991-01, Vol.56 (1), p.365-372

1991

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Thermal and trimethylsilyl triflate catalyzed additions of allylsilanes to nitrones

Journal of organic chemistry, 1988-04, Vol.53 (9), p.1957-1965

1988

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Cleavage of N ‘,N ‘-Dialkylhydrazides with PhI(OH)OTs

Organic letters, 2000-07, Vol.2 (14), p.2139-2140

2000

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Application of allylboronates to the synthesis of carbomycin B

Journal of organic chemistry, 1988-10, Vol.53 (21), p.5023-5034

1988

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Synthesis of the dipeptide hydroxyethylene isostere of Leu-Val, a transition state mimic for the control of enzyme function

Journal of organic chemistry, 1988-09, Vol.53 (19), p.4503-4508

1988

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Concentration Dependence of the Sharpless Asymmetric Amidohydroxylation of Isopropyl Cinnamate

Organic letters, 2000-08, Vol.2 (17), p.2667-2669

2000

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Bromine-Mediated Addition of Nucleophiles to the Electron-Rich Pyrimidine Subunit of Tirilazad

Journal of organic chemistry, 1994-08, Vol.59 (17), p.5090-5092

1994

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A new approach to the synthesis of the carbon framework of SC-84536, an inducible nitric oxide synthase inhibitor

Tetrahedron letters, 2008-06, Vol.49 (25), p.4033-4035

2008

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3-Acyltetramic acid antibiotics. 1. Synthesis of tirandamycic acid

Journal of the American Chemical Society, 1981-06, Vol.103 (11), p.3205-3207

1981

Volltextzugriff (PDF)

Improved Process for the Preparation of Tetrabutylammonium Anthracenesulfonate, a Precursor to Anthracenesulfonyl Chloride

Journal of organic chemistry, 1997-01, Vol.62 (2), p.430-430

Wuts, Peter G. M

1997

Volltextzugriff (PDF)

Stereoselective Alkylation of 7-Hydroxy-DHEA Derivatives

Synlett, 2007-09, Vol.2007 (14), p.2185-2188

2007

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Allylboronate synthesis. Synthesis of a .beta.-alkoxy carbanion equivalent

Journal of organic chemistry, 1983-12, Vol.48 (26), p.5398-5400

1983

Volltextzugriff (PDF)

Greene's protective groups in organic synthesis, fourth edition

4th ed., 2007

Volltextzugriff (PDF)

Stereoselective synthesis of racemic occidentalol and related cis-fused hexahydronaphthalenes from m-toluic acid

Journal of organic chemistry, 1977-05, Vol.42 (10), p.1794-1798

1977

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Novel riboswitch-binding flavin analog that protects mice against Clostridium difficile infection without inhibiting cecal flora

Continuous Flow Homolytic Aromatic Substitution with Electrophilic Radicals: A Fast and Scalable Protocol for Trifluoromethylation

Greene's Protective Groups in Organic Synthesis

Greene's Protective Groups in Organic Synthesis

Greene’s protective groups in organic synthesis, fifth edition

Generation of Broad-Spectrum Antifungal Drug Candidates from the Natural Product Compound Aureobasidin A

The Synthesis of Oxazolines Using the Vilsmeier Reagent

New Process for the Preparation of Methyl Carbonates

A Practical Synthesis of Cabergoline

Development of a practical synthesis of sumanirole

A Scalable Synthesis of the INOS Inhibitor PHA-399733

The addition of .gamma.-(trimethylsilyl)allylboronates to imines

Thermal and trimethylsilyl triflate catalyzed additions of allylsilanes to nitrones

Cleavage of N ‘,N ‘-Dialkylhydrazides with PhI(OH)OTs

Application of allylboronates to the synthesis of carbomycin B

Synthesis of the dipeptide hydroxyethylene isostere of Leu-Val, a transition state mimic for the control of enzyme function

Concentration Dependence of the Sharpless Asymmetric Amidohydroxylation of Isopropyl Cinnamate

Bromine-Mediated Addition of Nucleophiles to the Electron-Rich Pyrimidine Subunit of Tirilazad

A new approach to the synthesis of the carbon framework of SC-84536, an inducible nitric oxide synthase inhibitor

3-Acyltetramic acid antibiotics. 1. Synthesis of tirandamycic acid

Improved Process for the Preparation of Tetrabutylammonium Anthracenesulfonate, a Precursor to Anthracenesulfonyl Chloride

Stereoselective Alkylation of 7-Hydroxy-DHEA Derivatives

Allylboronate synthesis. Synthesis of a .beta.-alkoxy carbanion equivalent

Greene's protective groups in organic synthesis, fourth edition

Stereoselective synthesis of racemic occidentalol and related cis-fused hexahydronaphthalenes from m-toluic acid

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