A. Sercel

发表

Tyrosine kinase inhibitors. 16. 6,5,6-tricyclic benzothieno[3, 2-d]pyrimidines and pyrimido[5,4-b-] and -[4,5-b]ĭndoles as potent inhibitors of the epidermal growth factor receptor tyrosine kinase.

A. Bridges, D. W. Fry, H. D. Showalter, 1999, Journal of medicinal chemistry.

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 1. Thiazolone and oxazolone series.

R. D. Dyer, A. Sercel, K. Chan, 1999, Journal of medicinal chemistry.

R. D. Dyer, A. Sercel, R. Gilbertsen, 1999, Journal of medicinal chemistry.

Benzothiopyranoindazoles, a new class of chromophore modified anthracenedione anticancer agents. Synthesis and activity against murine leukemias.

H. D. Showalter, A. Sercel, D. Ortwine, 1988, Journal of medicinal chemistry.

Anticancer anthrapyrazoles. Improved syntheses of clinical agents CI‐937, CI‐941, and piroxantrone hydrochloride

H. D. Showalter, A. Sercel, C. Rithner, 1989 .

Annelation reactions of quinone monoketals. Studies directed at an efficient synthesis of anthracyclinones

A. Sercel, B. Chenard, J. S. Swenton, 1984 .

A convergent synthesis of (+)-4-demethoxydaunomycinone and ( + )-daunomycinone

A. Sercel, J. Freskos, G. W. Morrow, 1984 .

Anticancer Anthrapyrazoles. Improved Syntheses of Clinical Agents CI-937, CI-941, and Piroxantrone Hydrochloride.

H. D. Showalter, A. Sercel, C. Rithner, 1989 .

Efficient Synthesis of peri-Hydroxylated 9,10-Anthracenedione Ethers via Alkylation of Cesium Phenolates

H. D. Showalter, A. Sercel, R. T. Winters, 1988 .

The synthesis of symmetrical (2-indolyl)ethynes and reduced congeners via palladium-catalyzed couplings of 2-bromoindole precursors

H. D. Showalter, A. Sercel, 2006 .

Fluorous affinity purification of oligonucleotides.

A. Sercel, D. Berry, W. H. Pearson, 2005, The Journal of organic chemistry.

Pyrrolo-dC and pyrrolo-C: fluorescent analogs of cytidine and 2′-deoxycytidine for the study of oligonucleotides ☆

A. Sercel, D. Berry, J. B. Randolph, 2004 .

Synthesis of 3,4‐dihydro‐1(2H)‐isoquinolinonesxs

H. D. Showalter, A. Sercel, M. Stier, 2001 .

Tyrosine kinase inhibitors. 6. Structure-activity relationships among N- and 3-substituted 2,2'-diselenobis(1H-indoles) for inhibition of protein tyrosine kinases and comparative in vitro and in vivo studies against selected sulfur congeners.

W. Denny, D. W. Fry, H. D. Showalter, 1997, Journal of medicinal chemistry.

R. D. Dyer, A. Sercel, K. Chan, 1999, Journal of medicinal chemistry.

Simple Synthesis of 4‐Substituted 1(2H)‐Isoquinolinones via Electrophilic Trapping of Lithiated Mono‐ and Dianion Precursors

A. Sercel, J. P. Sanchez, H. D. Hollis Showalter, 2007 .

Simple Synthesis of 4‐Substituted 1(2H)‐Isoquinolinones via Electrophilic Trapping of Lithiated Mono‐ and Dianion Precursors.

H. D. Showalter, A. Sercel, J. P. Sanchez, 2008 .

Synthesis of 3,4‐Dihydro‐1(2H)‐isoquinolinones.

H. D. Showalter, A. Sercel, M. Stier, 2001 .

Erratum: Synthesis of 3,4-dihydro-1(2H)-isoquinolinones (Journal of Heterocyclic Chemistry (2000) 38 (961))

H. D. Showalter, A. Sercel, M. Stier, 2001 .

Synthesis of the enantiomers of the dual function 2‐nitroimidazole radiation sensitizer RB 6145

H. D. Showalter, A. Sercel, A. Michel, 2006 .

Tyrosine kinase inhibitors. 4. Structure-activity relationships among N- and 3-substituted 2,2'-dithiobis(1H-indoles) for in vitro inhibition of receptor and nonreceptor protein tyrosine kinases.

W. Denny, G. Rewcastle, D. W. Fry, 1995, Journal of medicinal chemistry.

Anticancer activity in murine and human tumor cell lines of bis(platinum) complexes incorporating straight-chain aliphatic diamine linker groups.

H. D. Showalter, A. Sercel, W. Elliott, 1992, Journal of medicinal chemistry.

Facile synthesis of thioglucose analogs of the anticancer agent etoposide

A. Sercel, R. T. Winters, A. Michel, 1991 .

The Synthesis of Symmetrical (2-Indolyl)ethynes and Reduced Congeners via Palladium-Catalyzed Couplings of 2-Bromoindole Precursors.

H. D. Showalter, A. Sercel, 2006 .

2,6-di-tert-butylphenols: A new class of potent and selective PGHS-2 inhibitor

R. D. Dyer, A. Sercel, K. Chan, 1997, Inflammation Research.