T. Tschamber

发表

Conformational analysis of some pyridinium phenolates and synthetic precursors based on X-ray and IR characterisations

M. Neuburger, C. Carre, V. Diemer, 2014 .

A NOVEL PORPHYRIN ISOMER: HEMIPORPHYCENE. FORMATION AND SINGLE-CRYSTAL X-RAY DIFFRACTION STRUCTURE DETERMINATION OF A HEMIPORPHYCENE NICKEL COMPLEX

H. Callot, B. Metz, A. Rohrer, 1995 .

Stereocontrolled synthesis of imidazolo[1,5]hexopiperidinoses and imidazol-4(5)-yl-C-glycosides

M. Neuburger, F. Gessier, S. Jankowski, 2003 .

Carbohydrate transition state mimics: synthesis of imidazolo-pyrrolidinoses as potential nectrisine surrogates.

M. Neuburger, C. Tarnus, F. Gessier, 2003, Bioorganic & medicinal chemistry.

Synthesis of Imidazolo‐Piperidinopentoses as Nagstatine Analogues

M. Neuburger, W. Huber, C. Tarnus, 2001 .

Single and double asymmetric induction in Diels-Alder cycloadditions with chiral acylnitroso dienophiles

D. Bur, A. Defoin, J. Streith, 1991 .

A Torquospecific 1,5‐Electrocyclization

A. Riesen, J. Streith, T. Tschamber, 1987 .

Ring-rearrangement metathesis of 3,6-dialkoxy-3,6-dihydro-2H-pyrans

S. Desrat, T. Tschamber, J. Eustache, 2008 .

Stereospecific double glycolisation of 1,2-dihydropyridines with OsO4. Synthesis of (±) aminoarabinose- and of (±) aminoaltrose derivatives [1].

J. Streith, T. Tschamber, F. Backenstrass, 1990 .

Stereoselective synthesis of D,L-erythrose-, and of D,L-1,4-dideoxy-4-aminoerythrose derivatives bearing a β-lactam at C-4

M. Muller, J. Streith, T. Tschamber, 1996 .

The Synthesis of Imidazol Sugars Which Mimic Cyclic Carboxonium Ions Formed During the Glycosidase‐Catalysed Hydrolysis of Oligo and Polysaccharides

C. Tarnus, H. Rudyk, J. Streith, 1999 .

Synthesis of Substituted Imidazolo[1,2‐a]piperidinoses and Their Evaluation as Glycosidase Inhibitors

C. Tarnus, D. L. Nouën, J. Streith, 2006 .

Asymmetric Synthesis of Diazepino‐β‐lactams by [2 + 2] Cycloaddition of an ‘Evans‐Sjogven’ Ketene with 1H‐1,2‐Diazepines

D. Bur, M. Muller, J. Streith, 1991 .

Stereocontrolled synthesis of enantiomeric imidazolopiperidinoses and imidazoloazepanoses using Wittig/dihydroxylation reactions

W. Wolf, C. Tarnus, E. Salomon, 2007 .

Rearrangement of N-substituted porphyrins. Preparation and structure of homoporphyrins

H. Callot, T. Tschamber, 1975 .

A simple asymmetric synthesis of 2-substituted 2,3-dihydro-4-pyridones

T. Sifferlen, J. Streith, T. Tschamber, 1994 .

Reaction of pyrylium salts with hydrazine and methylhydrazine. Concerning the scope of the 1,2(4H)-diazepine synthesis

V. Snieckus, T. Tschamber, G. Kan, 1980 .

Stereospecific Synthesis of 2‐Oxazinyl‐4‐oxoazetidinecarbamates Starting from a 1,2‐Diazepine. A new type of intramolecular transbenzoylation

J. Henlin, H. Fritz, A. Riesen, 1988 .

Stereoisomeric Imidazolo‐Pentoses − Synthesis, Chiroptical Properties, and Evaluation as Glycosidase Inhibitors

A. Aubertin, F. Gessier, H. Steiner, 2001 .

Stereocontrolled Synthesis of an Epimer of the C(19)‐to‐C(27) Segment of Rifamycin S

T. Tschamber, C. Tamm, N. Waespe‐Šarčevic̀, 1986 .

On the Way to Glycoprocessing Inhibitors. Synthesis of an imidazo‐L‐xylo‐piperidinose derivative

D. L. Nouën, J. Streith, T. Tschamber, 1995 .

Homoporphyrins II thermal rearrangements

H. Callot, T. Tschamber, 1974 .

Rotamerism-driven large magnitude host-guest binding change in a crown ether derivatized pyridinium-phenolate series.

D. Versace, M. Jin, Emel Ay, 2016, Chemical communications.

Catalytic One‐Pot Osmylation of Cyclohexadienes: Stereochemical and conformational studies of the resulting polyols

H. Fritz, J. Streith, T. Tschamber, 1992 .

Concerning restricted rotations in pyridinyl anisoles and pyridinyl phenols bearing saturated handles, and their solid state structures

M. Neuburger, Emel Ay, H. Chaumeil, 2014 .

Stereoselective catalytic double osmylation of 1,2-dihydropyridines leading to amino-arabinose and to amino-altrose derivatives and to potential glycosidase inhibitors.

T. Tschamber, M. Zehnder, M. Neuburger, 1994 .

Stereomeric Pyrrolidinopentoses Bearing an Imidazole Ring − Synthesis, Chiroptical Properties, and Evaluation as Potential Sugar-Mimic Glycosidase Inhibitors

C. Tarnus, J. Streith, T. Tschamber, 2002 .

Chelate‐Controlled Asymmetric Synthesis of 2‐Substituted 2,3‐Dihydropyridin‐4(1H)‐ones: Synthesis of D‐ and L‐aminodeoxyaltrose derivatives

J. Paillaud, E. Rodriguez‐Perez, J. Streith, 1995 .

Stereoselective Catalytic Double Osmylation of 1,2-Dihydropyridines leading to Aminoarabinose and to Aminoaltrose Derivatives and to Potential Glycosidase Inhibitors.

J. Streith, T. Tschamber, M. Zehnder, 1994 .

Soft Photopolymerizations Initiated by Dye-Sensitized Formation of NHC-Boryl Radicals under Visible Light

B. Graff, J. Fouassier, J. Lalevée, 2013 .

De novo Synthesis of Racemic Altronolactam and Arabinonolactam Azasugars.

E. Rodriguez‐Perez, J. Streith, T. Tschamber, 1996 .

On the Way to Glycoprocessing Inhibitors: A General One-Pot Synthesis of Imidazolosugars

H. Rudyk, D. L. Nouen, J. Streith, 1995 .

Chelate-Controlled Asymmetric Synthesis of 2-Substituted 2,3- Dihydropyridin-4(1H)-ones: Synthesis of D- and L-Aminodeoxyaltrose Derivatives.

J. Paillaud, E. Rodriguez‐Perez, J. Streith, 1995 .

Increasing the inhibitory potency of l-arabino-imidazolo-[1,2]-piperidinose towards β-d-glucosidase and β-d-galactosidase

J. Streith, T. Tschamber, E. Dubost, 2003 .

Ring-rearrangement metathesis of substituted dihydropyrans and dihydrofurans

S. Desrat, D. L. Nouen, T. Tschamber, 2011 .

On the synthesis, characterization and reactivity of N-heteroaryl-boryl radicals, a new radical class based on five-membered ring ligands.

D. Gigmes, J. Fouassier, J. Lalevée, 2014, Chemistry.

Synthesis of an imidazolo-L-lyxo-piperidinose derivative

J. Streith, T. Tschamber, A. Frankowski, 1998 .

Improved double epimerisation of (D)-glucose into (D)-gulose and the synthesis of (D)-xylo-imidazolopiperidinose

J. Streith, T. Tschamber, H. Siendt, 1999 .

Synthesis of an Imidazolo‐L‐lyxo‐piperidinose Derivative.

J. Streith, T. Tschamber, A. Frankowski, 1998 .

Synthesis and antitumor activity of the estrane analogue of OSW-1

H. Nemoto, Y. Matsuya, T. Tschamber, 2005 .

OSW-1 analogues: modification of the carbohydrate moiety.

H. Nemoto, Y. Matsuya, T. Tschamber, 2007, Bioorganic & medicinal chemistry letters.

Homoporphyrins I preparation - structure

H. Callot, T. Tschamber, 1974 .

Acid catalyzed isomerization and thermal rearrangement of nickel homoporphyrins

H. Callot, T. Tschamber, E. Schaeffer, 1975 .

Synthesis and Structure of a Cyclopropapyridine

H. Fritz, R. Bambal, J. Streith, 1987 .

Single and Double Asymmetric Induction in Diels‐Alder Cycloadditions with Chiral Acylnitroso Dienophiles.

D. Bur, A. Defoin, J. Streith, 1992 .