K. A. Sullivan

发表

Synthesis of indolo[2,3-a]carbazole glycoside analogs of rebeccamycin: inhibitors of cyclin D1-CDK4

M. Faul, K. A. Sullivan, J. Grutsch, 2004 .

1,7-annulated indolocarbazoles as cyclin-dependent kinase inhibitors.

S. A. Watkins, C. D. Spencer, N. Stamm, 2004, Bioorganic & medicinal chemistry letters.

Development of an Alternate Synthesis for a Key JAK2 Inhibitor Intermediate via Sequential C–H Bond Functionalization

K. A. Sullivan, J. R. Martinelli, S. May, 2013 .

A detailed study of the diastereoselective catalytic hydrogenation of 6-hydroxytetrahydroisoquinoline-(3R)-carboxylic ester intermediates

Todd D. Maloney, K. A. Sullivan, D. Ager, 2012 .

A novel, stereoselective synthesis of cis,4a (S), 8a(R)-decahydro-6(2H)-isoquinolones from meroquinene esters

M. Martinelli, K. A. Sullivan, B. Peterson, 1993 .

Macrocyclic Bisindolylmaleimides: Synthesis by Inter- and Intramolecular Alkylation

M. Faul, K. A. Sullivan, L. L. Winneroski, 1998 .

Synthetic approaches to indolo[6,7-a]pyrrolo[3,4-c]carbazoles: potent cyclin D1/CDK4 inhibitors.

S. W. Pedersen, M. Martinelli, J. M. Pawlak, 2004, The Journal of organic chemistry.

An Enantioselective Synthesis of Cis Perhydroisoquinoline LY235959.

M. Martinelli, K. A. Sullivan, M. M. Hansen, 1998, The Journal of organic chemistry.

Process Development for a Key Synthetic Intermediate of LY2140023, a Clinical Candidate for the Treatment of Schizophrenia

Michael E. Laurila, Cheryl A. Bye, K. A. Sullivan, 2011 .

1,7-annulated indolocarbazoles as cyclin-dependent kinase inhibitors.

S. A. Watkins, C. D. Spencer, N. Stamm, 2004, Bioorganic & medicinal chemistry letters.

Strategies for the synthesis of N-(azacycloalkyl)bisindolylmaleimides: selective inhibitors of PKCβ

Michael A. Staszak, M. Faul, K. A. Sullivan, 2003 .

Synthesis of cis-4a(S),8a(R)-Perhydro-6(2H)-Isoquinolinones from Quinine: 4a(S), 8a(R)-2-Benzoyloctahydro-6(2H)-Isoquinolinone

M. Martinelli, K. A. Sullivan, B. Peterson, 2003 .

A Novel, Stereoselective Synthesis of cis-4a(S),8a(R)-Decahydro-6(2H)- isoquinolones from Meroquinene Esters.

M. Martinelli, K. A. Sullivan, B. Peterson, 1994 .

5-Formyl salicylaldehyde as a linker for the synthesis of benzofuran containing insulin sensitivity enhancer compounds

K. A. Sullivan, J. Ward, J. Stille, 1996 .

Novel, potent and selective cyclin D1/CDK4 inhibitors: indolo[6,7-a]pyrrolo[3,4-c]carbazoles.

S. A. Watkins, R. Campbell, J. Dempsey, 2003, Bioorganic & medicinal chemistry letters.

Phenyliodine(III) bis(trifluoroacetate)-mediated oxidation of bisindolylmaleimides to indolo[2,3-a]carbazoles

M. Faul, K. A. Sullivan, 2001 .

Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitors.

S. A. Watkins, R. Schultz, Faming Zhang, 2004, Bioorganic & medicinal chemistry letters.

Mitigating the Risk of Coprecipitation of Pinacol during Isolation from Telescoped Miyaura Borylation and Suzuki Couplings Utilizing Boron Pinacol Esters: Use of Modeling for Process Design

J. M. Merritt, K. A. Sullivan, Rachel N. Richey, 2016 .

Selective Monoarylation of Benzenediols via Dianion Intermediates

Michael E. Laurila, K. A. Sullivan, C. Xie, 2007 .

Synthesis of novel retinoid X receptor-selective retinoids.

M. Faul, K. A. Sullivan, L. L. Winneroski, 2001, The Journal of organic chemistry.

Synthesis of Novel Retinoid X Receptor‐Selective Retinoids.

M. Faul, K. A. Sullivan, L. L. Winneroski, 2001 .

Synthesis of aryl- and heteroaryl[a]pyrrolo[3,4-c]carbazoles.

M. Faul, K. A. Sullivan, J. Grutsch, 2003, The Journal of organic chemistry.

A General Approach to the Synthesis of Bisindolylmaleimides: Synthesis of Staurosporine Aglycone

M. Faul, K. A. Sullivan, L. L. Winneroski, 1995 .

Synthesis of Aryl‐ and Heteroaryl[a]pyrrolo[3,4‐c]carbazoles.

M. Faul, K. A. Sullivan, J. Grutsch, 2004 .