J. Mcnamara

发表

A diastereospecific, non-racemic synthesis of a novel β-hydroxy-δ-lactone HMG-CoA reductase inhibitor

R. Volante, E. Corley, M. Sletzinger, 1985 .

Synthesis of a potent hNK-1 receptor antagonist via an SN2 reaction of an enantiomerically pure alpha-alkoxy sulfonate.

J. Payack, M. Huffman, J. Mcnamara, 2005, Organic letters.

A regioselective synthesis of 2,4-dialkyl resorcinols

J. Mcnamara, S. Ceglia, T. Nelson, 2005 .

A very concise synthesis of a potent N-(1,3-thiazol-2-yl)pyridin-2-amine KDR kinase inhibitor

M. Huffman, Jingjun Yin, J. Mcnamara, 2006 .

Pd-catalyzed N-arylation of heteroarylamines.

M. Huffman, Jingjun Yin, J. Mcnamara, 2002, Organic letters.

A convenient synthesis of 3-aryl-δ-lactones

M. Huffman, J. Mcnamara, T. Nelson, 2003 .

Asymmetric bioreduction of benzyl acetoacetate to its corresponding alcohol, benzyl (S)-(+)-3-hydroxybutyrate by the yeast Candida schatavii MY 1831

M. Chartrain, R. Greasham, J. Mcnamara, 1996 .

Effective use of preparative chiral HPLC in a preclinical drug synthesis.

C. Welch, D. Mathre, M. Huffman, 2004, Chirality.

A concise synthesis of a novel antiangiogenic tyrosine kinase inhibitor.

Enrique Vazquez, J. Payack, J. Mcnamara, 2005, The Journal of organic chemistry.

Practical chemoenzymatic synthesis of a 3-pyridylethanolamino β3 adrenergic receptor agonist

Edward J. J. Grabowski, David L. Hughes, John Leazer, 1999 .

One-Pot Preparation of 7-Hydroxyquinoline

A. Figus, J. Mcnamara, M. Cameron, 2006 .

Practical routes to the triarylsulfonyl chloride intermediate of a β3 adrenergic receptor agonist

P. Reider, Jinchu Liu, J. Mcnamara, 2003 .

Practical asymmetric synthesis of aklavinone

Y. Kishi, J. Mcnamara, 1982 .

Practical asymmetric syntheses of 11-deoxydaunomycinone and related compounds

Y. Kishi, J. Mcnamara, H. Sekizaki, 1982 .

Pseudoephedrine as a chiral auxiliary for asymmetric Michael reactions: synthesis of 3-aryl-delta-lactones.

P. Reider, M. Huffman, J. Murry, 2002, Organic letters.

Efficient synthesis of NK(1) receptor antagonist aprepitant using a crystallization-induced diastereoselective transformation.

Jing Li, Paul N Devine, Paul N. Devine, 2003, Journal of the American Chemical Society.

Reductive decyanation of pyrazinecarbonitriles

M. D. Baker, P. Dormer, J. Mcnamara, 2002 .

Practical total synthesis of (.+-.)-aklavinone and total synthesis of aklavin

B. A. Pearlman, Y. Kishi, S. Hatakeyama, 1981 .

Stereoselective synthesis of a potent thrombin inhibitor by a novel P2-P3 lactone ring opening.

Jeffrey C. Moore, M. Sturr, K. Gbewonyo, 2004, The Journal of organic chemistry.

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

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

Highly Chemoselective Trichloroacetimidate-Mediated Alkylation of Ascomycin: A Convergent, Practical Synthesis of the Immunosuppressant L-733,725.

Yulan Li, D. Mathre, P. Reider, 1999, The Journal of organic chemistry.

Process Development and Large-Scale Synthesis of a PDE4 Inhibitor

D. Deschěnes, D. Macdonald, R. Helmy, 2006 .

A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

A. W. Douglas, D. Mathre, P. Reider, 1996 .

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

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

Syntheses of morpholine-2,3-diones and 2-hydroxymorpholin-3-ones: intermediates in the synthesis of aprepitant

M. Huffman, J. Mcnamara, K. Brands, 2004 .

Practical asymmetric synthesis of aprepitant, a potent human NK-1 receptor antagonist, via a stereoselective Lewis acid-catalyzed trans acetalization reaction.

P. Reider, E. Grabowski, Guojie Ho, 2002, The Journal of organic chemistry.

Efficient Synthesis of a Highly Selective NPY-5 Receptor Antagonist: A Drug Candidate for the Treatment of Obesity

K. Maeda, N. Nonoyama, T. Itoh, 2006 .

Asymmetric hydrogenation of 3-alkylidene-2-piperidones using Noyori's catalyst. Effect of N-substituents on the enantioselectivity

P. Reider, E. Grabowski, Dalian Zhao, 1995 .

Asymmetric Hydrogenation of 3-Alkylidene-2-piperidones Using Noyori′s Catalyst. Effect of N-Substituents on the Enantioselectivity.

P. Reider, E. Grabowski, Dalian Zhao, 1996 .

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

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

Aluminum-Amine Complexes for the Conversion of Carboxylic Esters to Amides. Application to the Synthesis of LTD4 Antagonist MK-0679

D. Sidler, P. Reider, J. Mcnamara, 1994 .

Aluminum‐Amine Complexes for the Conversion of Carboxylic Esters to Amides. Application to the Synthesis of LTD4 Antagonist MK‐0679.

D. Sidler, P. Reider, J. Mcnamara, 1994 .