A. Toró

发表

2,3,4,5-Tetrahydro-1H-pyrido[2,3-b and e][1,4]diazepines as inhibitors of the bacterial enoyl ACP reductase, FabI.

David D. Manning, P. Sampson, N. Kaplan, 2009, Bioorganic & medicinal chemistry letters.

Development of 4H-pyridopyrimidines: a class of selective bacterial protein synthesis inhibitors

U. Ochsner, J. Bullard, J. Guiles, 2012, Organic and medicinal chemistry letters.

Structure and mechanism of action of the hydroxy aryl aldehyde class of IRE 1 endoribonuclease inhibitors

G. Poda, D. Durocher, F. Sicheri, 2015 .

Structure and mechanism of action of the hydroxy aryl aldehyde class of IRE1 endoribonuclease inhibitors

G. Poda, D. Durocher, F. Sicheri, 2014, Nature Communications.

Facile Synthesis of Methyl 2-Formyl-5-hydroxymethyl-3-furancarboxylate

P. Deslongchamps, A. Toró, 1999 .

The transannular Diels-Alder strategy: applications to total synthesis

É. Marsault, P. Nowak, P. Deslongchamps, 2001 .

Transannular Diels−Alder Entry into Stemodanes: First Asymmetric Total Synthesis of (+)-Maritimol

A. Nowak, P. Deslongchamps, A. Toró, 2000 .

Potent nonpeptide antagonists of the bradykinin B1 receptor: structure-activity relationship studies with novel diaminochroman carboxamides.

Ming Huang, Hong Sun, Eileen Johnson, 2007, Journal of medicinal chemistry.

Transannular Diels-Alder studies on the asymmetric total synthesis of chatancin: the pyranophane approach.

P. Deslongchamps, A. L’Heureux, A. Toró, 2000, Organic letters.

Transannular Diels–Alder Studies of 14-Membered cis–trans–trans Macrocyclic Trienes Having Allylic Ether or Enone Dienophile

S. Ouellet, Y. Dory, P. Deslongchamps, 2000 .

Transannular Diels-Alder studies on the asymmetric synthesis of (+)-maritimol

P. Deslongchamps, A. Toró, G. Bélanger, 1999 .

Development of a Bleaching Process for a Kaolin of Industrial Interest by Oxalic, Ascorbic, and Sulfuric Acids: Preliminary Study Using Statistical Methods of Experimental Design

F. Vegliò, A. Marabini, A. Toró, 1996 .

Pyranophane transannular diels-alder approach to (+)-chatancin: a biomimetic asymmetric total synthesis.

P. Soucy, P. Deslongchamps, A. L’Heureux, 2003, The Journal of organic chemistry.

Furanophane transannular Diels-Alder approach to (+)-chatancin: an asymmetric total synthesis of (+)-anhydrochatancin.

P. Deslongchamps, A. Toró, 2003, The Journal of organic chemistry.

Transannular Diels-Alder model studies on the total synthesis of chatancin. The furanophane approach. Part 2 [1]: Macrocyclization and Diels-Alder reaction

M. Drouin, Y. Wang, P. Deslongchamps, 1999 .

Transannular Diels-Alder model studies on the total synthesis of chatancin. The furanophane approach. Part 1: Assembly of the acyclic substrates

Y. Wang, P. Deslongchamps, A. Toró, 1999 .

Pyranophane Transannular Diels—Alder Approach to (+)‐Chatancin (I): A Biomimetic Asymmetric Total Synthesis.

P. Soucy, P. Deslongchamps, A. L’Heureux, 2004 .

Furanophane Transannular Diels—Alder Approach to (+)‐Chatancin: An Asymmetric Total Synthesis of (+)‐Anhydrochatancin.

P. Deslongchamps, A. Toró, 2004 .

Transannular Diels—Alder Model Studies on the Total Synthesis of Chatancin. The Furanophane Approach. Part 1. Assembly of the Acyclic Substrates.

P. Deslongchamps, A. Toró, Yuan-Lin Wang, 1999 .

Transannular Diels—Alder Model Studies on the Total Synthesis of Chatancin. The Furanophane Approach. Part 2. Macrocyclization and Diels—Alder Reaction.

M. Drouin, P. Deslongchamps, A. Toró, 1999 .

Synthesis of chiral trans-syn-cis and trans-anti-trans [6.6.6] tricycles by transannular Diels-Alder reaction

P. Deslongchamps, R. Lavoie, A. Toró, 1999 .

MACROCYCLIZATION OF TERMINAL BIS-ALLYLIC CHLORIDES VIA AN INTRAMOLECULAR GEM-DIALKYLATION OF MALONONITRILE OR METHYL CYANOACETATE

Y. Chantigny, P. Deslongchamps, A. Toró, 1998 .

Use of the transannular DielsAlder (TADA) reaction to probe biological receptors: Rational design and synthesis of tricyclic TADA adducts capable of rigidly holding pharmacophore parts

Y. Chantigny, Y. Dory, P. Deslongchamps, 2002 .

Oxidative decarboxylation of 17(20)-dehydro-2,324-dinorcholanoic acids

G. Ambrus, A. Toró, 1990 .

Identification of a nonpeptidic and conformationally restricted bradykinin B1 receptor antagonist with anti-inflammatory activity.

L. Arik, E. Laird, V. Viswanadhan, 2007, Journal of medicinal chemistry.

The mechanism of the gibbs reaction. Part 2: The ortho ⇉ ortho 2,4-cyclohexadiene-1-one rearrangement of the reaction product of 2,6-di-tert-butyl-4-chlorophenol and 2,6-dichlorobenzoquinone N-chloroimine

A. Toró, I. Pallagi, József Müller, 1994 .

Mechanism of the Gibbs Reaction. 3. Indophenol Formation via Radical Electrophilic Aromatic Substitution (SREAr) on Phenols

Ö. Farkas, A. Toró, I. Pallagi, 1994 .