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Crystal structure of N-tosyl-2-methylserine, C11H15NO5S

Zeitschrift für Kristallographie. New crystal structures, 2010-03, Vol.225 (1), p.139-140

2010

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Crystal structure of N-tosyl-2-methylserine-β-lactone, C11H13NO4S

Zeitschrift für Kristallographie. New crystal structures, 2010-03, Vol.225 (1), p.137-138

2010

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Crystal structure of N-((2R,4S)-2-tert-butyl-5-methyl-4H- 1,3-dioxin-4-yl)-2-(trimethylsilyl)ethanesulfonamide, C14H29NO4Si

Zeitschrift für Kristallographie. New crystal structures, 2007-06, Vol.222 (2), p.139-140

2007

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Crystal structure of N-((2R,4S)-2-tert-butyl-5-methyl-4H- 1,3-dioxin-4-yl)-2-(trimethylsilyl)ethanesulfonamide, C14H29NO4Si

Zeitschrift für Kristallographie. New crystal structures, 2007-06, Vol.222 (2), p.139-140

2007

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Crystal structure of (2R,4S)-methyl 2-isopropyl-4-methyl-3-(2-(trimethylsilyl) ethylsulfonyl)-1,3-oxazolidine-4-carboxylate, C14H29NO5SSi

Zeitschrift für Kristallographie. New crystal structures, 2007-06, Vol.222 (2), p.141-142

2007

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Crystal structure of (2R,4S)-methyl 2-isopropyl-4-methyl-3-(2-(trimethylsilyl) ethylsulfonyl)-1,3-oxazolidine-4-carboxylate, C14H29NO5SSi

Zeitschrift für Kristallographie. New crystal structures, 2007-06, Vol.222 (2), p.141-142

2007

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Asymmetric synthesis of 4H-1,3-dioxins and investigations in the metal catalyzed aziridination: aziridination versus insertion and stereoselective course

ARKIVOC, 2007-03, Vol.2007 (10), p.245-259

2007

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The absolute configuration of (2S,4S)- and (2R,4R)-2-tert-butyl-4-methyl-3-(4-tolylsulfonyl)-1,3-oxazolidine-4-carbaldehyde

Acta crystallographica. Section C, Crystal structure communications, 2006-02, Vol.62 (2), p.o101-o103

2006

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The endo and exo isomers of 1-(4-isopropyl-3,5-dioxa-8-azabicyclo[5.1.0]octan-8-yl)pyrrolidine-2,5-dione

Acta crystallographica. Section C, Crystal structure communications, 2005-12, Vol.61 (12), p.o705-o706

2005

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5-Methyl-4H-1,3-dioxins, new chiral building blocks: transformation into (R)- and (S)-4-hydroxymethyl-4-methyl-1,3-dioxolanes via oxidation and rearrangement and determination of the absolute configuration

Tetrahedron: asymmetry, 2005-10, Vol.16 (20), p.3394-3399

2005

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5-Methyl-4 H-1,3-dioxins, new chiral building blocks: transformation into ( R)- and ( S)-4-hydroxymethyl-4-methyl-1,3-dioxolanes via oxidation and rearrangement and determination of the absolute configuration

Tetrahedron: asymmetry, 2005, Vol.16 (20), p.3394-3399

2005

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Crystal structure of 4-acetoxy-5-(amino-N-phthalimido)-2-tert-butyl-5- methyl-1,3-dioxane, C19H24N2O6

Zeitschrift für Kristallographie. New crystal structures, 2004-04, Vol.219 (1), p.303-304

2004

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Crystal structure of 4-acetoxy-5-(amino-N-phthalimido)-2-tert-butyl-5-methyl-1,3-dioxane, C19H24N2O6

Zeitschrift für Kristallographie. New crystal structures, 2004, Vol.219 (3), p.283-284

2004

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ChemInform Abstract: Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products

ChemInform, 2001-04, Vol.32 (16), p.no-no

2001

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Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products This work was supported by the Fonds der Chemische Industrie. We would like to thank Prof. Dr. H. Brunner, Universität Regensburg, for help in questions concerning analytical data. Me-DuPHOS=1,2-bis(2,5-dimethylphospholanyl)benzene

Angewandte Chemie (International ed.), 2001-01, Vol.40 (1), p.177-179

2001

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Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products

Angewandte Chemie (International ed.), 2001-01, Vol.40 (1), p.177-179

2001

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Die hochenantioselektive katalytische Doppelbindungsisomerisierung von 4,7‐Dihydro‐1,3‐dioxepinen mit Me‐DuPHOS‐modifizierten Dihalogenonickel‐Komplexen und Bestimmung der Absolutkonfiguration der Isomerisierungsprodukte

Angewandte Chemie, 2001-01, Vol.113 (1), p.176-178

2001

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Die hochenantioselektive katalytische Doppelbindungsisomerisierung von 4,7-Dihydro-1,3-dioxepinen mit Me-DuPHOS-modifizierten Dihalogenonickel-Komplexen und Bestimmung der Absolutkonfiguration der Isomerisierungsprodukte

Angewandte Chemie, 2001-01, Vol.113 (1), p.176-178

2001

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Aziridination of 5-Methyl-4H-1,3-dioxins by N-Tosyliminophenyliodinane: A One-step Procedure for the Synthesis of α-Methylserinal Derivatives

Synlett, 2001, Vol.2001 (6), p.0839-0841

2001

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ChemInform Abstract: A Novel Synthesis of 4-Methyl-1,3-dioxolane-4-carbaldehydes by Epoxidation of 5-Methyl-4H-1,3-dioxines and Acid-Catalyzed Rearrangement

ChemInform, 1999-07, Vol.30 (27), p.no-no

1999

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A Novel Synthesis of 4-Methyl-1,3-Dioxolane-4-Carbaldehydes by Epoxidation of 5-Methyl-4 H -1,3-Dioxins and Acid-Catalyzed Rearrangement

Synlett, 1999-03, Vol.1999 (3), p.303-306

1999

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A Novel Synthesis of 4-Methyl-1,3-Dioxolane-4-Carbaldehydes by Epoxidation of 5-Methyl-4H-1,3-Dioxins and Acid-Catalyzed Rearrangement

Synlett, 1999, Vol.1999 (3), p.303-306

1999

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Asymmetric double-bond isomerization of cyclic allyl acetals by using diop and chiraphos modified nickel complexes

Tetrahedron: asymmetry, 1998-04, Vol.9 (7), p.1103-1106

1998

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A Highly Z-Selective Isomerization (Double-Bond Migration) Procedure for Allyl Acetals and Allyl Ethers Mediated by Nickel Complexes

Synthesis (Stuttgart), 1998-03, Vol.1998 (3), p.305-308

1998

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9.12 - 1,4-Dioxepanes, 1,4-Oxathiepanes, and 1,4-Dithiepanes

Comprehensive Heterocyclic Chemistry II, 1996, p.271-297

Frauenrath, Herbert

Second Edition, 1996

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Crystal structure of N-tosyl-2-methylserine, C11H15NO5S

Crystal structure of N-tosyl-2-methylserine-β-lactone, C11H13NO4S

Crystal structure of N-((2R,4S)-2-tert-butyl-5-methyl-4H- 1,3-dioxin-4-yl)-2-(trimethylsilyl)ethanesulfonamide, C14H29NO4Si

Crystal structure of N-((2R,4S)-2-tert-butyl-5-methyl-4H- 1,3-dioxin-4-yl)-2-(trimethylsilyl)ethanesulfonamide, C14H29NO4Si

Crystal structure of (2R,4S)-methyl 2-isopropyl-4-methyl-3-(2-(trimethylsilyl) ethylsulfonyl)-1,3-oxazolidine-4-carboxylate, C14H29NO5SSi

Crystal structure of (2R,4S)-methyl 2-isopropyl-4-methyl-3-(2-(trimethylsilyl) ethylsulfonyl)-1,3-oxazolidine-4-carboxylate, C14H29NO5SSi

Asymmetric synthesis of 4H-1,3-dioxins and investigations in the metal catalyzed aziridination: aziridination versus insertion and stereoselective course

The absolute configuration of (2S,4S)- and (2R,4R)-2-tert-butyl-4-methyl-3-(4-tolylsulfonyl)-1,3-oxazolidine-4-carbaldehyde

The endo and exo isomers of 1-(4-isopropyl-3,5-dioxa-8-azabicyclo[5.1.0]octan-8-yl)pyrrolidine-2,5-dione

5-Methyl-4H-1,3-dioxins, new chiral building blocks: transformation into (R)- and (S)-4-hydroxymethyl-4-methyl-1,3-dioxolanes via oxidation and rearrangement and determination of the absolute configuration

5-Methyl-4 H-1,3-dioxins, new chiral building blocks: transformation into ( R)- and ( S)-4-hydroxymethyl-4-methyl-1,3-dioxolanes via oxidation and rearrangement and determination of the absolute configuration

Crystal structure of 4-acetoxy-5-(amino-N-phthalimido)-2-tert-butyl-5- methyl-1,3-dioxane, C19H24N2O6

Crystal structure of 4-acetoxy-5-(amino-N-phthalimido)-2-tert-butyl-5-methyl-1,3-dioxane, C19H24N2O6

ChemInform Abstract: Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products

Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products

Die hochenantioselektive katalytische Doppelbindungsisomerisierung von 4,7‐Dihydro‐1,3‐dioxepinen mit Me‐DuPHOS‐modifizierten Dihalogenonickel‐Komplexen und Bestimmung der Absolutkonfiguration der Isomerisierungsprodukte

Die hochenantioselektive katalytische Doppelbindungsisomerisierung von 4,7-Dihydro-1,3-dioxepinen mit Me-DuPHOS-modifizierten Dihalogenonickel-Komplexen und Bestimmung der Absolutkonfiguration der Isomerisierungsprodukte

Aziridination of 5-Methyl-4H-1,3-dioxins by N-Tosyliminophenyliodinane: A One-step Procedure for the Synthesis of α-Methylserinal Derivatives

ChemInform Abstract: A Novel Synthesis of 4-Methyl-1,3-dioxolane-4-carbaldehydes by Epoxidation of 5-Methyl-4H-1,3-dioxines and Acid-Catalyzed Rearrangement

A Novel Synthesis of 4-Methyl-1,3-Dioxolane-4-Carbaldehydes by Epoxidation of 5-Methyl-4 H -1,3-Dioxins and Acid-Catalyzed Rearrangement

A Novel Synthesis of 4-Methyl-1,3-Dioxolane-4-Carbaldehydes by Epoxidation of 5-Methyl-4H-1,3-Dioxins and Acid-Catalyzed Rearrangement

Asymmetric double-bond isomerization of cyclic allyl acetals by using diop and chiraphos modified nickel complexes

A Highly Z-Selective Isomerization (Double-Bond Migration) Procedure for Allyl Acetals and Allyl Ethers Mediated by Nickel Complexes

9.12 - 1,4-Dioxepanes, 1,4-Oxathiepanes, and 1,4-Dithiepanes

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