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Reaction of Pertechnetate in Highly Alkaline Solution: Synthesis and Characterization of the Nitridotrioxotechnetate Ba[TcO3N]

Chemistry : a European journal, 2022-11, Vol.28 (63), p.e202201738-n/a

2022

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Enantiopure Monoprotected cis-1,2-Diaminocyclohexane: One-Step Preparation and Application in Asymmetric Organocatalysis

ChemCatChem, 2010-10, Vol.2 (10), p.1215-1218

2010

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Control of asymmetric biaryl conformations with terpenol moieties: syntheses, structures and energetics of new enantiopure C2-symmetric diols

Beilstein journal of organic chemistry, 2008-07, Vol.4 (1), p.25-25

2008

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An exceptional P-H phosphonite: biphenyl-2,2'-bisfenchylchlorophosphite and derived ligands (BIFOPs) in enantioselective copper-catalyzed 1,4-additions

Beilstein journal of organic chemistry, 2005-08, Vol.1 (1), p.6-6

2005

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The Chiral Pool as Valuable Natural Source: New Chiral Mesogens Made From Lactic Acid

Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003), 2011-01, Vol.542 (1), p.62/[584]-74/[596]

2011

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Cover Picture: Enantiopure Monoprotected cis-1,2-Diaminocyclohexane: One-Step Preparation and Application in Asymmetric Organocatalysis (ChemCatChem 10/2010)

ChemCatChem, 2010-10, Vol.2 (10), p.1177-1177

2010

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Enantioselective Synthesis of Bicyclo[4.4.1]undecane-2,7-dione via Samarium(II)-Mediated Fragmentation of a Cyclopropane Precursor

Synlett, 2006-06, Vol.2006 (10), p.1527-1530

2006

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Synthesis and Structural Characterization of a New Class of Strong Chiral Brønsted Acids: 1,1′-Binaphthyl-2,2′-bis(sulfuryl)imides (JINGLEs)

European Journal of Organic Chemistry, 2010-09, Vol.2010 (27), p.5165-5170

2010

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New chiral lithium aluminum hydrides based on biphenyl-2,2′-bisfenchol (BIFOL): structural analyses and enantioselective reductions of aryl alkyl ketones

Tetrahedron, 2006-04, Vol.62 (15), p.3704-3709

2006

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The Chiral Pool as Valuable Natural Source: New Chiral Mesogens Made From Lactic Acid

Molecular Crystals and Liquid Crystals, 2011-06, Vol.542 (1), p.584

2011

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Enantioselective Synthesis of DIANANE, a Novel C 2-Symmetric Chiral Diamine for Asymmetric Catalysis

Journal of organic chemistry, 2004-04, Vol.69 (9), p.3050-3056

2004

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A Family of New 1,2,4-Trioxanes by Photooxygenation of Allylic Alcohols in Sensitizer-Doped Polymers and Secondary Reactions

Synthesis (Stuttgart), 2005-09, Vol.2005 (14), p.2433-2444

2005

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Umpolung by N-Heterocyclic Carbenes: Generation and Reactivity of the Elusive 2,2-Diamino Enols (Breslow Intermediates)

Angewandte Chemie (International ed.), 2012-12, Vol.51 (49), p.12370-12374

International ed. in English, 2012

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Iodine-Catalyzed Nazarov Cyclizations

Journal of organic chemistry, 2019-06, Vol.84 (12), p.7587-7605

2019

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( Z )-3-(4-Methoxybenzylidene)-2-methylisoindolin-1-one

Acta crystallographica. Section E, Structure reports online, 2005-04, Vol.61 (4), p.o1074-o1075

2005

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Breslow Intermediates (Amino Enols) and Their Keto Tautomers: First Gas‐Phase Characterization by IR Ion Spectroscopy

Chemistry : a European journal, 2021-02, Vol.27 (8), p.2662-2669

2021

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Hydrogen Bonding Shuts Down Tunneling in Hydroxycarbenes: A Gas-Phase Study by Tandem-Mass Spectrometry, Infrared Ion Spectroscopy, and Theory

Journal of the American Chemical Society, 2023-06, Vol.145 (22), p.12124-12135

2023

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Redetermination of the solvent-free crystal structure of l-proline

Acta crystallographica. Section E, Crystallographic communications, 2018-08, Vol.74 (Pt 8), p.1067-1070

2018

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N‐(2‐Phenethyl)phthalimide

Acta crystallographica. Section E, Structure reports online, 2006-04, Vol.62 (4), p.o1580-o1581

2006

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Cover Feature: Breslow Intermediates (Amino Enols) and Their Keto Tautomers: First Gas‐Phase Characterization by IR Ion Spectroscopy (Chem. Eur. J. 8/2021)

Chemistry : a European journal, 2021-02, Vol.27 (8), p.2552-2552

2021

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Titelbild: Umpolung mit N-heterocyclischen Carbenen: Generierung und Reaktivität von Breslow-Intermediaten (2,2-Diaminoenole) (Angew. Chem. 49/2012)

Angewandte Chemie, 2012-12, Vol.124 (49), p.12301-12301

2012

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Umpolung mit N-heterocyclischen Carbenen: Generierung und Reaktivität von Breslow-Intermediaten (2,2-Diaminoenole)

Angewandte Chemie, 2012-12, Vol.124 (49), p.12537-12541

2012

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Hydrogen tunneling avoided: enol-formation from a charge-tagged phenyl pyruvic acid derivative evidenced by tandem-MS, IR ion spectroscopy and theory

Physical chemistry chemical physics : PCCP, 2019, Vol.21 (3), p.16591-166

2019

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Cover Picture: Umpolung by N-Heterocyclic Carbenes: Generation and Reactivity of the Elusive 2,2-Diamino Enols (Breslow Intermediates) (Angew. Chem. Int. Ed. 49/2012)

Angewandte Chemie (International ed.), 2012-12, Vol.51 (49), p.12135-12135

2012

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(538) - Ischemia Reperfusion Injury Significantly Differs Between Lung vs. Heart Transplantation with Respect to Lead Cytokines and Correlation to Clinical Outcome

The Journal of heart and lung transplantation, 2018-04, Vol.37 (4), p.S219-S220

2018

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Reaction of Pertechnetate in Highly Alkaline Solution: Synthesis and Characterization of the Nitridotrioxotechnetate Ba[TcO3N]

Enantiopure Monoprotected cis-1,2-Diaminocyclohexane: One-Step Preparation and Application in Asymmetric Organocatalysis

Control of asymmetric biaryl conformations with terpenol moieties: syntheses, structures and energetics of new enantiopure C2-symmetric diols

An exceptional P-H phosphonite: biphenyl-2,2'-bisfenchylchlorophosphite and derived ligands (BIFOPs) in enantioselective copper-catalyzed 1,4-additions

The Chiral Pool as Valuable Natural Source: New Chiral Mesogens Made From Lactic Acid

Cover Picture: Enantiopure Monoprotected cis-1,2-Diaminocyclohexane: One-Step Preparation and Application in Asymmetric Organocatalysis (ChemCatChem 10/2010)

Enantioselective Synthesis of Bicyclo[4.4.1]undecane-2,7-dione via Samarium(II)-Mediated Fragmentation of a Cyclopropane Precursor

Synthesis and Structural Characterization of a New Class of Strong Chiral Brønsted Acids: 1,1′-Binaphthyl-2,2′-bis(sulfuryl)imides (JINGLEs)

New chiral lithium aluminum hydrides based on biphenyl-2,2′-bisfenchol (BIFOL): structural analyses and enantioselective reductions of aryl alkyl ketones

The Chiral Pool as Valuable Natural Source: New Chiral Mesogens Made From Lactic Acid

Enantioselective Synthesis of DIANANE, a Novel C 2-Symmetric Chiral Diamine for Asymmetric Catalysis

A Family of New 1,2,4-Trioxanes by Photooxygenation of Allylic Alcohols in Sensitizer-Doped Polymers and Secondary Reactions

Umpolung by N-Heterocyclic Carbenes: Generation and Reactivity of the Elusive 2,2-Diamino Enols (Breslow Intermediates)

Iodine-Catalyzed Nazarov Cyclizations

( Z )-3-(4-Methoxybenzylidene)-2-methylisoindolin-1-one

Breslow Intermediates (Amino Enols) and Their Keto Tautomers: First Gas‐Phase Characterization by IR Ion Spectroscopy

Hydrogen Bonding Shuts Down Tunneling in Hydroxycarbenes: A Gas-Phase Study by Tandem-Mass Spectrometry, Infrared Ion Spectroscopy, and Theory

Redetermination of the solvent-free crystal structure of l-proline

N‐(2‐Phenethyl)phthalimide

Cover Feature: Breslow Intermediates (Amino Enols) and Their Keto Tautomers: First Gas‐Phase Characterization by IR Ion Spectroscopy (Chem. Eur. J. 8/2021)

Titelbild: Umpolung mit N-heterocyclischen Carbenen: Generierung und Reaktivität von Breslow-Intermediaten (2,2-Diaminoenole) (Angew. Chem. 49/2012)

Umpolung mit N-heterocyclischen Carbenen: Generierung und Reaktivität von Breslow-Intermediaten (2,2-Diaminoenole)

Hydrogen tunneling avoided: enol-formation from a charge-tagged phenyl pyruvic acid derivative evidenced by tandem-MS, IR ion spectroscopy and theory

Cover Picture: Umpolung by N-Heterocyclic Carbenes: Generation and Reactivity of the Elusive 2,2-Diamino Enols (Breslow Intermediates) (Angew. Chem. Int. Ed. 49/2012)

(538) - Ischemia Reperfusion Injury Significantly Differs Between Lung vs. Heart Transplantation with Respect to Lead Cytokines and Correlation to Clinical Outcome

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