J. Amato

发表

Process development for the production of the (S)-acid precursor of a novel elastase inhibitor (L-694,458) through the lipase-catalyzed kinetic resolution of a β-lactam benzyl ester

M. Chartrain, R. Greasham, V. Pecore, 1997 .

Cyclization of electrochemically generated nitrogen radicals.

E. Corley, N. L. Abramson, S. Karady, 1991 .

High temperature reactions of benzene

R. Firestone, J. Amato, 1970 .

A NEW PREPARATION OF CHLOROMETHYL METHYL ETHER FREE OF BIS(CHLOROMETHYL) ETHER

S. Karady, J. Amato, M. Sletzinger, 1979 .

Annelation of aromatic oxo compounds

R. Reamer, S. Karady, J. Amato, 1996 .

Stereospecific conversion of penicillin to thienamycin

R. Reamer, S. Karady, J. Amato, 1981 .

Stereospecific conversion of penicillin to thienamycin

R. Reamer, S. Karady, J. Amato, 1981 .

An Asymmetric Synthesis of L-694,458, a Human Leukocyte Elastase Inhibitor, via Novel Enzyme Resolution of beta-Lactam Esters.

M. Chartrain, E. Grabowski, Christopher Roberge, 1996, The Journal of organic chemistry.

Acylimidazolides as Versatile Synthetic Intermediates for the Preparation of Sterically Congested Amides and Ketones: A Practical Synthesis of Proscar®

E. Grabowski, J. Amato, A. Bhattacharya, 1990 .

An Efficient and Scalable Process for the Preparation of a Potent MC4 Receptor Agonist

E. Corley, R. Reamer, John Y. L. Chung, 2007 .

Practical Syntheses of 13-O-[(2-Methoxyethoxy)methyl]-22,23-dihydroavermectin B1 Aglycon [Dimedectin Isopropanol, MK-324] and 13-epi-O-(Methoxymethyl)-22,23-Dihydroavermectin B1 Aglycon [L-694,554], Flea Active Ivermectin Analogues

C. Senanayake, E. Grabowski, R. Shuman, 1997 .

An Efficient Synthesis of a Dual PPAR α/γ Agonist and the Formation of a Sterically Congested α-Aryloxyisobutyric Acid via a Bargellini Reaction

John Y. L. Chung, R. Cvetovich, J. Amato, 2005 .

Enantioselective nitrile anion cyclization to substituted pyrrolidines. A highly efficient synthesis of (3S,4R)-N-tert-butyl-4-arylpyrrolidine-3-carboxylic acid.

R. Reamer, John Y. L. Chung, J. McWilliams, 2005, The Journal of organic chemistry.

Oxime Formation of 4''-epi-(Acetylamino)-5-oxo-4''-deoxy-avermectin B1

E. Grabowski, R. Reamer, R. Shuman, 1994 .

Lipase-Catalyzed Asymmetric Hydrolysis of Esters Having Remote Chiral/Prochiral Centers

D. Sidler, P. Reider, E. Grabowski, 1990 .

1,2,5-Thiadiazole 1-oxides. 3. An experimental and theoretical investigation of the inversion barrier

J. Springer, H. Schlegel, R. Reamer, 1982 .

1,2,5-thiadiazole-1-oxides, IV, ring transformation to 1,2,3,5-thiatriazole- and 1,2,4,6-thiatriazene-1-oxide

R. Reamer, S. Karady, J. Amato, 1985 .

Lipase-Catalyzed Asymmetric Hydrolysis of Esters Having Remote Chiral/ Prochiral Centers.

D. Sidler, P. Reider, E. Grabowski, 1991 .

DEVELOPMENT OF THE HOFMANN REARRANGEMENT OF NALPHA -TOSYLASPARAGINE THROUGH CALORIMETRIC AND NMR ANALYSIS

R. Reamer, R. Cvetovich, J. Amato, 1998 .

1,2,5-THIADIAZOLE-1-OXIDES. II. THE CHEMISTRY OF THE AMINES

D. Dortmund, S. Karady, J. Amato, 1981 .

Utilization of .alpha.,.beta.-unsaturated acids as Michael acceptors for the synthesis of thieno[2,3-b]thiopyrans

M. Holloway, G. Ponticello, J. Baldwin, 1988 .

Synthesis of chiral dithioacetals: a chemoenzymic synthesis of a novel LTD4 antagonist

P. Reider, E. Grabowski, J. Amato, 1989 .

Conversion of imidoyl chlorides to imines. A new method for the acyl exchange and cleavage of amides

S. Karady, J. Amato, M. Sletzinger, 1978 .

Synthesis of Unsymmetrical Dithioacetals: An Efficient Synthesis of a Novel LTD4 Antagonist, L-660,711

P. Reider, E. Grabowski, R. Reamer, 1989 .