Audrey Molina

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Synthesis of a new generation reverse transcriptase inhibitor via the BCl3/GaCl3-induced condensation of anilines with nitriles (sugasawa reaction)

A. W. Douglas, I. Houpis, Audrey Molina, 1994 .

In situ NMR spectroscopic studies of aniline ortho acylation (“sugasawa reaction”): The nature of reaction intermediates and Lewis acid influence on yield

A. W. Douglas, I. Houpis, Audrey Molina, 1994 .

A practical synthesis of the 5-chloromethyl-furo[2,3-b]pyridine pharmacophore

I. Houpis, Audrey Molina, P. Reider, 1995 .

Synthesis of functionalized furo[2,3-b]pyridines via the Pd-catalyzed coupling of acetylenes to iodopyridones. Preparation of a key intermediate to a new HIV protease inhibitor L-754,394

I. Houpis, Audrey Molina, J. Lynch, 1994 .

Condensation of 2-methylbenzoxazole with aromatic aldehydes bearing acidic protons. A convenient coupling in the synthesis of the HIV-reverse transcriptase inhibitor L-696,229

I. Houpis, Audrey Molina, J. Lynch, 1993 .

Synthesis of the orally active spiroindoline-based growth hormone secretagogue, MK-677

K. Rossen, I. Houpis, Audrey Molina, 1997 .

Ni-catalyzed nucleophilic conjugate additions of Grignard and organozincate reagents to substituted 4-vinylpyridines. General synthesis of phosphodiesterase IV inhibitors

I. Houpis, Audrey Molina, R. Volante, 1998 .

Synthesis of hypusine and other polyamines using dibenzyltriazones for amino protection

S. Knapp, Audrey Molina, Kuang Yu Chen, 1992 .

Nickel catalyzed addition of organozincates to optically pure vinylic sulfoxides. Synthesis of the phosphodiesterase IV inhibitor L-765,527 (CDP-840)

I. Houpis, Audrey Molina, R. Volante, 1997 .

Towards the synthesis of HIV-protease inhibitors. Synthesis optically pure 3-carboxyl-decahydroisoquinolines.

I. Houpis, Audrey Molina, R. Volante, 1993 .

A Practical Synthesis of the 5‐Chloromethyl‐furo(2,3‐b)pyridine Pharmacophore.

I. Houpis, Audrey Molina, R. Volante, 1995 .

The Palladium Catalyzed Coupling of β-Trifuoromethanesulfonyl α,β-Unsaturated Esters and Ketones with β-Stannyl Enoates: Synthesis of Electron Deficient Dienes

I. Houpis, Audrey Molina, L. Dimichele, 1993 .

Design, Synthesis, and Biological Activity of Substrate Competitive SMYD2 Inhibitors.

N. Keen, A. Ferguson, J. Pietenpol, 2016, Journal of medicinal chemistry.

Discovery of 6-aryl-azabenzimidazoles that inhibit the TBK1/IKK-ε kinases.

C. Chuaqui, Hai‐Jun Zhang, Audrey Molina, 2014, Bioorganic & medicinal chemistry letters.

Discovery of 6-aryl-azabenzimidazoles that inhibit the TBK1/IKK-ε kinases.

C. Chuaqui, Hai‐Jun Zhang, Audrey Molina, 2014, Bioorganic & medicinal chemistry letters.

Synthesis of a New Generation Reverse Transcriptase Inhibitor via the BCl3/GaCl3‐Induced Condensation of Anilines with Nitriles (Sugasawa Reaction).

A. W. Douglas, I. Houpis, Audrey Molina, 1995 .