Russell J. Thomas

发表

Identification of 2-aminopyrimidine derivatives as inhibitors of the canonical Wnt signaling pathway.

Arianna Nencini, T. Benicchi, F. Del Bello, 2015, Bioorganic & medicinal chemistry.

JPET #49395 1 PHARMACOLOGY OF (2S,4Z)-N-[(2S)-2-HYDROXY-2-PHENYLETHYL]-4- (METHOXYIMINO)-1-[(2’-METHYL[1,1’-BIPHENYL]-4-YL)CARBONYL]-2- PYRROLIDINECARBOXAMIDE, A NEW POTENT AND SELECTIVE NON- PEPTIDE ANTAGONIST OF THE OXYTOCIN RECEPTOR

C. Giachetti, A. Nichols, C. Barberis, 2003 .

Pharmacology of (2S,4Z)-N-[(2S)-2-Hydroxy-2-phenylethyl]-4-(methoxyimino) -1-[(2′-methyl[1,1′-biphenyl]-4-yl)carbonyl]-2-pyrrolidinecarboxamide, a New Potent and Selective Nonpeptide Antagonist of the Oxytocin Receptor

C. Giachetti, M. Schwarz, A. Scheer, 2003, Journal of Pharmacology and Experimental Therapeutics.

The renewed challenge of antibacterial chemotherapy

L. Tarsi, Russell J. Thomas, D. Niccolai, 1998 .

The stereoselective synthesis of 4-formyltrinem, a key intermediate for novel trinems

C. Ghiron, T. Rossi, Russell J. Thomas, 1997 .

Nitrate ester derivatives from epoxides using CAN: Efficient preparation of key intermediates in the synthesis of 4-alkoxytrinems

R. Fabio, T. Rossi, Russell J. Thomas, 1997 .

Stereoselective Synthesis of a Key Intermediate of Sanfetrinem by Means of a Chelated Tin(IV) Enolate

A. Paio, P. Zarantonello, T. Rossi, 1997 .

The stereoselective synthesis of a key intermediate of the trinem antibiotic sanfetrinem

C. Ghiron, T. Rossi, Russell J. Thomas, 1996 .

NOVEL AMIDOALKYLATION OF 4-ACETOXYAZETIDINONES WITH ALLYLIC BORANES. A STEREOSELECTIVE ENTRY INTO THE TRIBACTAMS

T. Rossi, C. Marchioro, S. Biondi, 1995 .

The synthesis of a key intermediate of tricyclic beta-lactam antibiotics

D. Donati, R. Fabio, T. Rossi, 1995 .

The synthesis of 4-aminocarbonylmethoxy trinems

Barbara Bertani, P. Zarantonello, C. Ghiron, 1997 .

Nitrate Ester Derivatives from Epoxides Using CAN: Efficient Preparation of Key Intermediates in the Synthesis of 4-Alkoxytrinems.

R. Fabio, T. Rossi, Russell J. Thomas, 1997 .

The Stereoselective Synthesis of a Key Intermediate of the Trinem Antibiotic Sanfetrinem.

C. Ghiron, T. Rossi, Russell J. Thomas, 1996 .

Stereoselective Synthesis of a Key Intermediate of Sanfetrinem by Means of a Chelated Tin(IV) Enolate.

A. Paio, P. Zarantonello, T. Rossi, 1997 .

Novel Amidoalkylation of 4-Acetoxyazetidinones with Allylic Boranes. A Stereoselective Entry into the Tribactams.

T. Rossi, C. Marchioro, S. Biondi, 1996 .

The Stereoselective Synthesis of 4‐Formyltrinem, a Key Intermediate for Novel Trinems.

C. Ghiron, T. Rossi, Russell J. Thomas, 1997 .

The Synthesis of a Key Intermediate of Tricyclic β-Lactam Antibiotics.

D. Donati, R. Fabio, T. Rossi, 1995 .

The Synthesis of 4-Aminocarbonylmethoxy Trinems.

Barbara Bertani, P. Zarantonello, C. Ghiron, 1998 .

Some reactions of 2-azabicycio[2.2.1]hept-5-enes with diphenylketene: preparation of polysubstituted piperidin-2-ones

S. Roberts, Russell J. Thomas, Smith Colin William, 1990 .

Some unexpected reactions involving diphenylketene

S. Roberts, R. Maurya, R. J. Pryce, 1992 .

The asymmetric synthesis of both enantiomers of eliprodil

C. Pietra, R. Fabio, L. Ziviani, 1995 .

Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists.

C. Giachetti, M. Schwarz, A. Scheer, 2005, Journal of medicinal chemistry.

Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1.

P. Distefano, M. Navia, J. Hixon, 2005, Journal of medicinal chemistry.

Fruitful adrenergic α(2C)-agonism/α(2A)-antagonism combination to prevent and contrast morphine tolerance and dependence.

U. Zanelli, L. Mattioli, M. Giannella, 2010, Journal of medicinal chemistry.