V. Jäger

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Crystal structure of (2S, 3R, 4S, 5R)-2-methylpiperidine-1,3,4,5-tetrol hydrochloride, C6H14ClNO4

W. Frey, Jeanne Heller, V. Jäger, 2012 .

Crystal structure of (N,N',N"-trimethyl-N,N',N"-tris-(1-phenylethyl)- guanidinium hexafluorophosphate), C28H36F6N3P

W. Frey, V. Jäger, A. Castiglia, 2012 .

Crystal structure of (2S, 3S, 4R, 5S)-3,4-dihydroxy-5-methyl-2-nonylpyrrolidine hydrochloride, C14H30ClNO2

V. Jäger, Et al., 2012 .

Crystal structure of (2S, 3S, 4R, 5S)-2-(4-iodophenyl)-3,4-Oisopropylidene- 5-methyl-1,3,4-trihydroxypyrrolidine, C14H18INO3

W. Frey, V. Jäger, A. Castiglia, 2012 .

Crystal structure of rel-(3aS,6aS)-3-(4-methoxyphenyl)- 4,6a-dihydro-3aH-cyclopenta[d]isoxazole, C13H13NO2

J. Lee, W. Frey, V. Jäger, 2005 .

Crystal structure of 1,3,5-tris(4-methoxyphenyl)-1H-1,2,4-triazole-2- oxide, C23H21N3O4

W. Frey, J. Lee, V. Jäger, 2005 .

Crystal structure of 1,3,5-tris(4-methoxyphenyl)-1H-1,2,4-triazole-2- oxide, C23H21N3O4

J. Lee, W. Frey, V. Jäger, 2005 .

Synthesis of L-Furanomycin and Its Analogues via Furoisoxazolines†

R. Endermann, Iva Hlobilová, P. Zimmermann, 2005 .

Stereocontrol in isoxazoline reductions. Synthesis of aminodeoxy-DL-xylo- and arabino-pentose derivatives from furoisoxazolines

E. Paulus, V. Jäger, I. Müller, 1985 .

Synthesis of proteasome inhibitor 6-deoxy-omuralide and its enantiomer using stereoselective alkylation of substituted proline ester.

Feng Li, V. Jäger, 2020, Organic & biomolecular chemistry.

3‐ and 4‐Uloses Derived from N‐Acetyl‐D‐glucosamine: A Unique Pair of Complementary Organocatalysts for Asymmetric Epoxidation of Alkenes

V. Jäger, C. Schöberl, 2012 .

Asymmetric sharpless epoxidation of divinylcarbinol. Erythro-D- and -L-4-pentenitols by hydrolysis of regioisomeric epoxy-4-pentenols☆☆☆

B. Koppenhoefer, V. Jäger, Detlef Schröter, 1991 .

Auxiliary-controlled diastereoselection by N-(1-phenylethyl) in Grignard additions to 2-O-benzylglyceraldehyde imines

U. Vieth, V. Jäger, S. Leurs, 1996 .

Synthesis of optically active hydroxy amino acids via 2-O-benzylglyceraldehyde N-[(R)-1-phenylethyl]imine

N. Meunier, U. Vieth, V. Jäger, 1996 .

Synthesis of amino sugars via isoxazolines

V. Jäger, I. Müller, 1985 .

Synthesis of amino sugars via isoxazolines: DL- and D-lividosamine (2-amino-2,3-dideoxy-ribo-hexose) derivatives from 4-vinyl-1,3-dioxolanes and nitroacetaldehyde acetals

V. Jäger, R. Schohe, 1984 .

Simple and versatile synthesis of optically active 1,2-amino alcohols by Grignard addition to N,O-dibenzylglyceraldimine and -lactaldimine

K. Peters, U. Veith, E. Peters, 1994 .

A New Synthesis of 1,3,4‐Trideoxy‐1,4‐iminoglycitols of Varying Chain Length by (C3 + Cn)‐Coupling of Allyl Halides with Glycononitrile Oxides

R. Müller, M. Pätzel, V. Jäger, 1994 .

GLYCONO-1,3-LACTAMS, XYLO SERIES : STEREOSELECTIVE ACCESS BY 2+2 CYCLOADDITION, EXPLORATORY TRANSFORMATIONS, AND DISCOVERY OF A NEW, HIGHLY SELECTIVE INHIBITOR OF GLUCOAMYLASES

V. Jäger, S. Picasso, B. Krämer, 1997 .

A General Approach toL-(+)-Furanomycin and Some Stereoisomers and Analogues Using Furoisoxazoline Intermediates

P. Zimmermann, V. Jäger, I. Blanarikova, 2000 .

Stereoselective nitrile oxide cycloadditions to chiral allyl ethers and alcohols. The inside alkoxy effect

K. Houk, Yundong Wu, F. Fronczek, 1984 .

Pd(II)‐Catalyzed Carbonylation of Unsaturated Polyols and Aminopolyols

L. Remeň, A. Lieberknecht, T. Gracza, 1999 .

Synthesis of amino sugars via isoxazolines the concept and one application: nitrile oxide/furan adducts

V. Jäger, I. Müller, 1982 .

Model Reactions for the Stereo‐Controlled Synthesis of Aminopolyols; Reduction of Isoxazolines with Free or Protected Hydroxy Groups in Position 4 or in Side Chains

W. Schwab, V. Buss, V. Jäger, 1981 .

Synthesis of 3,5-Anhydro-2-deoxy-1,4-glyconolactones by Palladium(II)-Catalyzed, Regioselective Oxycarbonylation of C5- and C6-Enitols. ω-Homologation of Aldoses to Produce Intermediates for C-Glycoside/C-Nucleoside Synthesis

T. Gracza, V. Jäger, T. Hasenöhrl, 1991 .

Halocyclization and Palladium(II)-Catalyzed Amidocarbonylation of Unsaturated Aminopolypols. Synthesis of 1,4-Iminoglycitols as Potential Glycosidase Inhibitors

T. Gracza, V. Jäger, E. Dubois, 1997 .

Controlled Synthesis of Enantio-, Regio-, and Diastereomers of Amino-4-pentenediols from 1,4-Pentadien-3-ol via Epoxy-4-pentenols I. erythro-1-Amino-4-pentene-2,3-diols

T. Gracza, V. Jäger, W. Hümmer, 1991 .

Regiocontrol in the synthesis of optically active amino-4-pentenediols via epoxy-4-pentenols. Novel acyclic adenosine analogues☆

T. Gracza, V. Jäger, W. Hümmer, 1989 .

Synthesis of Glycosidase‐Inhibiting Iminopolyols Via Isoxazolines1,2

M. Hein, R. Müller, M. Pätzel, 2010 .

Stereoselective 1,3-dipolar cycloadditions to heterocyclic compounds

Ľ. Fišera, V. Ondruš, J. Kubáň, 2000 .

New heterocyclic structures from unsaturated aldehyde derivatives. Inhibition of α-L-fucosidases

W. Frey, Han-Qing Dong, V. Jäger, 2000 .

Amino(hydroxymethyl)cyclopentanetriols, an Emerging Class of Potent Glycosidase Inhibitors—Part II: Synthesis, Evaluation, and Optimization of β‐D‐Galactopyranoside Analogues

V. Jäger, S. Picasso, B. Schneider, 2001, Chembiochem : a European journal of chemical biology.

3-Nitropropanal and 3-nitropropanol: preparation of the parent compounds and derivatives

W. Schwab, V. Jäger, R. Ehrler, 1986 .

Nitrile oxide cycloadditions to olefinated sugars

P. Colinas, A. Lieberknecht, R. D. Bravo, 2003 .

Cationic cyclization of linalyl- and geranyl/nerylacetic acid. A facile entry to the brexane system

J. Buddrus, V. Jäger, W. Kuhn, 1986 .

Synthesis of erythro‐D‐ and ‐L‐4‐Pentenetriols. Selective Epoxy Allyl Alcohol Hydrolysis with Retention or Twofold Inversion (Enantiomerization)

V. Jäger, Detlef Schröter, Brigitte Häfele, 1986 .

(−)‐2‐O‐Benzyl‐L‐Glyceraldehyde and Ethyl (R,E)‐4‐O‐Benzyl‐4,5‐Dihydroxy‐2‐Pentenoate

V. Wehner, A. Lieberknecht, V. Jäger, 2003 .

2‐O‐Benzylglyceraldehyde: A Synthetic Building Block Available in Both Enantiomeric Forms and Configurationally Stable Owing to Rapid Oligomerization

V. Wehner, V. Jäger, 1989 .

A Short Synthesis of (S)-5-Hydroxy-2-penten-4-olide from D-Mannitol via 2,3-O-Isopropylidene-D-glyceraldehyde

V. Jäger, Brigitte Häfele, 1987 .

Cycloadditionen Organometallfragment-substituierter Alkene. I: [3+2]-Cycloaddition von η1-allyl-Eisenkomplexen mit Nitriloxiden : Ferriomethyl-substituierte Isoxazoline

A. Arif, M. Schwarz, V. Jäger, 1994 .

Controlled Synthesis of Regio-, Enantio-, and Diastereomers of Amino-4-pentenediols from 1,4-Pentadien-3-ol via Epoxy-4-pentenols II. erythro- and threo-3-Amino-4-pentene-1,2-diols and erythro-2-Benzylamino-4-pentene-1,3-diol

V. Jäger, W. Hümmer, U. Stahl, 1991 .

Synthesis of iminopolyols via Henry reaction: a short route to the α-manno- sidase inhibitor 1,4-dideoxy-1,4-imino-D-mannitol and to amino analogues†,1

V. Jäger, S. Picasso, F.-M. Kieß, 1998 .

Synthesis of L-carbafuranomycin, an unnatural analogue of the antibiotic amino acid furanomycin.

G. Schiffer, V. Jäger, J. Lee, 2005, Organic letters.

Cyclization of N‐Protected l‐Amino‐4‐pentene‐2,3‐diols to lxyo‐Configurated Deoxyimino Sugars (cis‐Dihydroxypyrrolidines); Synthesis of Potential Glycosidase Inhibitors

V. Jäger, W. Hümmer, 1990 .

Nitroacetylen‐Additionen an Enamine und Inamine

V. Jäger, H. Viehe, 1970 .

(1′R)‐(−)‐2,4‐O‐Ethylidene‐D‐Erythrose and Ethyl (E)‐(−)‐4,6‐O‐Ethylidene‐(4S,5R,1′R)‐4,5,6‐Trihydroxy‐2‐Hexenoate

O. Schwardt, V. Jäger, B. Krämer, 2003 .

Isoxazolinium Salts in Asymmetric Synthesis. 1. Stereoselective Reduction Induced by a 3’-Alkoxy Stereocentre. A New Approach to Polyfunctionalized β-Amino Acids* [1, 2]

M. Henneböhle, M. Hein, V. Jäger, 2004 .

Isoxazolines‐Key Intermediates For Syntheses of Some Naturally Occuring Amino Compounds

W. Schwab, V. Buss, R. Franz, 2010 .

Syntheses via isoxazolines III. Diastereoselective synthesis of γ-amino-alcohols with 2 and 3 chiral centres☆☆☆

W. Schwab, V. Buss, V. Jäger, 1978 .

Syntheses via isoxazolines II. Novel 4-substituted 2-isoxazolines byendo-deprotonation/alkylation

W. Schwab, V. Jäger, 1978 .

Asymmetric induction in nitrile oxide cycloadditions to 3-butene-1,2-diol and derivatives

E. Paulus, V. Jäger, R. Schohe, 1983 .

Ring‐Opening of 5‐(Bromomethyl)‐2‐isoxazolines to β,γ‐Enoximes—A New Principle for the γ‐Substitution of Allyl Bromides by α‐Functionalized Alkyl Groups

W. Schwab, V. Jäger, H. Grund, 1979 .

Pyrrolidine N-Oxides by Stereoselective Addition of Grignard and Lithium Compounds to 4,5-Dideoxy-2,3-O-isopropylidene-D-erythro-4-pentenose N-Benzyl Nitrone and Subsequent Cope−House Cyclization

V. Jäger, A. Palmer, 2001 .

Preparation and Biological Evaluation of Pyrrolidinediols and Pyrrolidine N-Oxides from D-Ribose Using the Nitrone Approach

V. Jäger, A. Palmer, 2001 .

Stereoselective Synthesis and Biological Evaluation of Anisomycin and 2-Substituted Analogues

O. Schwardt, U. Veith, C. Gaspard, 1999 .

Crystal structure of (3S,4R,1'R,1''R)-3-acetoxy-4-[2''-acetoxyacetoxy-1'',-benzyloxy-ethyl]-1-(1'-phenylethyl)-azetidin-2-one,C26H29NO8

V. Jäger, S. Henkel, Β. Krämer, 1997 .

Crystal structure of (3S,4R,1'R)-3-hydroxy-4-(1',2'-dihydroxyethyl)-azetidin- 2-one, C5H9NO4

V. Jäger, S. Henkel, Β. Krämer, 1997 .

Crystal structure of (3S,4R,1'R)-1-benzyl-3-benzyloxy-4-(1'-benzyloxy-2'- hydroxyethyI)-azetidine-2-one, C26H27NO4

K. Peters, E. Peters, V. Jäger, 1997 .

Synthesis of D- and L-2-Amino-2-deoxyarabinose and 1,4-Dideoxy-1,4-iminolyxitol by (C2 + C3)-Nitroaldol Addition with 2-O-Benzylglyceraldehyde†‡

V. Wehner, V. Jäger, 1990 .

Amino(hydroxymethyl)cyclopentanetriols, an Emerging Class of Potent Glycosidase Inhibitors—Part I: Synthesis and Evaluation of β‐D‐Pyranoside Analogues in the manno, gluco, galacto, and GlcNAc Series

P. Vogel, Jing Li, V. Jäger, 2001, Chembiochem : a European journal of chemical biology.

Synthesis of γ-methylene butyrolactones (4-penten-4-olides)

H. J. Günther, V. Jäger, 1977 .

Crystal structure of (3aR,5S,6R,6aR)-6-hydroxy-5-hydroxymethyl-perhydrofuro[3,2-b]furan-2-one, C7H10O5

W. Frey, V. Jäger, T. Hasenöhrl, 1999 .

Crystal structure of (1S,3S,4R,7S)-7-benzyloxy-3-[(1S)-1-hydroxy-lphenylmethyl]-2,5-dioxabicyclo[2.2.1]heptane, C19H20O4

W. Frey, L. Remeň, T. Gracza, 1999 .

Crystal structure of (3aS,4R,5S,6R,6aS)-4,5,6-triacetoxy- 1-benzyl-3,3a,4,5,6,6a-hexahydro-1H-cyclopent[c]-isoxazole, C19H23NO7

J. Kubáň, V. Jäger, P. Pruschek, 1999 .

Synthesis of L‐Erythro‐α,β‐Dihydroxy‐GABA and γ‐Hydroxy‐L‐Erythronine by Oxidative Degradation of Amino‐4‐Pentenediols

V. Jäger, Bettina Kirschbaum, U. Stahl, 2010 .

Synthesis of Natural and Unnatural Enantiomers of Goniofufurone and Its 7-Epimers from D-Glucose. Application of Palladium(II) - Catalyzed Oxycarbonylation of Unsaturated Polyols

T. Gracza, V. Jäger, 1994 .

Synthesis of D-erythrose and D-threose derived nitrones and cycloadditions to styrene

V. Langer, Ľ. Fišera, N. Prónayová, 1999 .

On the stereoselectivity of nitrone addition to (R)4-0-benzyl-4-lide

Ľ. Fišera, V. Ondruš, J. Kubáň, 1995 .

Crystal structure of (2S,3R,4S,1’R,2'S)-3,4-dimethanesulfonyloxy- 2-[2,3-O-isopropylidenedioxy-1-(tert-butoxycarbonylamino)propyl]- 5,5-dimethyl-tetrahydrofuran, C19H35NO11S2

W. Frey, P. Zimmermann, V. Jäger, 2000 .

Total syntheses of (+)- and (−)-1-deoxynojirimycin (1,5-dideoxy-1,5-imino-d- and l-glucitol) and of (+)- and (−)-1-deoxyidonojirimycin (1,5-dideoxy-1,5-imino-d- and l-iditol) via furoisoxazoline-3-aldehydes

P. Vogel, C. Schaller, V. Jäger, 1998 .

Crystal structure of methyl-5-amino-6,7-O-cyclohexylidene-5-deoxy- 3O,5N-ethylidene-α-D-ido-L-glycero-hepto-furanoside, C16H27NO6

W. Frey, P. Zimmermann, V. Jäger, 1998 .

Crystal structure of(ЗaR,6aR)-3-[(1R,2S,3S)-1,3:2,4-di-O- ethylidene-1,2,3,4-tetrahydroxy-1-butyl]-Зa,6a-dihydrofuro[2,3-d]ίsoxazole, C13H17NO6

V. Jäger, T. Leibold, S. Henkel, 1998 .

4‐Hydroxylation of Isoxazolines; Synthesis of rac‐Phytosphingosine (ribo‐2‐Amino‐1,3,4‐octadecanetriol)

W. Schwab, V. Jäger, 1981 .

Eliminative Ring Opening of 2‐Isoxazolines: A New Route to α,β‐Unsaturated Ketones

V. Jäger, H. Grund, 1976 .

Palladium (II)-Catalyzed Oxycarbonylation of Unsaturated Polyols: Synthesis of (-)-Goniofufurone and Assignment of Absolute Configuration to the Natural (+)-Enantiomer, a Cytotoxic Styryllactone1

T. Gracza, V. Jäger, 1992 .

Concise Synthesis of Deacetylanisomycin and 2-Substituted Analogues from N,2-O-Dibenzyl-L-threose Imine1

O. Schwardt, U. Veith, V. Jäger, 1996 .

Crystal structure of α-D-gluco-5-(1,2-di-O-isopropylidene-3-O-methanesulfonyl- furanos-4-yl)-3-phenyl-2-isoxazoline, C17H21NO7S

K. Peters, E. Peters, H. Schnering, 1997 .

Crystal structure of methyl-α-D-gluco-5-(1,2-di-O-isopropyIidene-3-O- niethanesulfonyl-furanos-4-yl)-2-isoxazoline-3-carboxylate, C13H19NO9S

E. Peters, H. Schnering, D. Schäfer, 1997 .

Nitroacetaldehyde Diethyl Acetal

V. Jäger, P. Poggendorf, 2003 .

Addition of Nitroacetylenes to Enamines and Ynamines

V. Jäger, H. Viehe, 1970 .

CLINICAL USES OF 2,3-DIMERCAPTOPROPANOL (BAL). VII. THE TREATMENT OF ARSENICAL DERMATITIS WITH PREPARATIONS OF BAL.

M. Wintrobe, W. T. Longcope, J. Luetscher, 1946, The Journal of clinical investigation.

Crystal structure of (3aS,4R,5S,6R,6aS)-4,5,6-trihydroxy-5,6-O-isopropylidene-3,3a,4,5,6,6a-hexahydro-1H-cyclopent[c]isoxazole, C9H15NO4