R. J. Post

发表

The Evolution of High-Throughput Experimentation in Pharmaceutical Development and Perspectives on the Future

Ling Li, Emma McInturff, Ke Wang, 2019, Organic Process Research & Development.

A synthesis of 5‐carboxamidopyrrolo[3,2‐b]pyridine

K. Ryan, R. J. Post, E. MacorJohn, 1992 .

Ethoxymethylenemalonates and Malononitriles (EMM reagents) as formic acid equivalents: Synthesis of fused-imidazoles under neutral or mildly acidic con

J. Macor, B. Chenard, B. E. Segelstein, 1993 .

Development of an Efficient Pd-Catalyzed Coupling Process for Axitinib

R. Vaidyanathan, G. Sluggett, Brett M. Lillie, 2014 .

Synthesis and reactivity of pyrrolo[3,2-e]indole: Removal of a N-BOM group from an unactivated indole

K. Ryan, James T. Forman, R. J. Post, 1997 .

The synthesis of conformationally/rotationally restricted analogs of the neurotransmitter serotonin

D. H. Blank, R. J. Post, E. MacorJohn, 1994 .

Palbociclib Commercial Manufacturing Process Development. Part III. Deprotection Followed by Crystallization for API Particle Property Control

K. Leeman, N. Ide, Karen Sutherland, 2016 .

5-[(3-nitropyrid-2-yl)amino]indoles: novel serotonin agonists with selectivity for the 5-HT1D receptor. Variation of the C3 substituent on the indole template leads to increased 5-HT1D receptor selectivity.

Anne W. Schmidt, J. Macor, K. Ryan, 1994, Journal of medicinal chemistry.

A Direct Synthesis of 3-(Pyrrolidin-3-yl)indoles for Use As Conformationally Restricted Analogs of Tryptamines

J. Macor, K. Ryan, K. Ryan, 1997 .

5-cyano-1-[3-(N-methylpyrrolidin-2R-ylmethyl)indol-5-yl] benzimidazole (CP-161,242): A potent, centrally active 5-HT1D receptor agonist and benzodiazepine partial agonist

Anne W. Schmidt, P. Seymour, J. Macor, 1995 .