C. A. Zificsak

发表

Synthesis and biological evaluation of sulfonyl acrylonitriles as novel inhibitors to peritoneal carcinomatosis.

S. Kuwada, B. Dorsey, Joseph G Lisko, 2012, Bioorganic & medicinal chemistry letters.

Design, synthesis, and biological evaluation of sulfonyl acrylonitriles as novel inhibitors of cancer metastasis and spread.

J. Shea, B. Ruggeri, C. Scaife, 2015, Journal of medicinal chemistry.

Current Methods for the Synthesis of 2-Substituted Azoles

D. Hlasta, C. A. Zificsak, 2004 .

Cycloaddition reactions of thiazolium azomethine ylides: application to pyrrolo[2,1-b]thiazoles.

A. Gibbs, D. Hlasta, C. R. Berry, 2007, Organic letters.

Efficient preparations of novel ynamides and allenamides

R. Hsung, J. Mulder, C. Douglas, 2001 .

The first stereoselective Ficini-Claisen rearrangement using chiral ynamides.

R. Hsung, M. O. Frederick, J. Mulder, 2002, Organic letters.

A Formal [3 + 3] Cycloaddition Reaction. Improved Reactivity Using α,β-Unsaturated Iminium Salts and Evidence for Reversibility of 6π-Electron Electrocyclic Ring Closure of 1-Oxatrienes

R. Hsung, J. Liu, Hong C Shen, 2003 .

Intramolecular formal aza-[3 + 3] cycloaddition approach to indoloquinolizidine alkaloids. A stereoselective total synthesis of (+/-)-tangutorine.

R. Hsung, C. A. Zificsak, Shengjun Luo, 2003, Organic letters.

Recent Advances in the Chemistry of Ynamines and Ynamides

R. Hsung, J. Mulder, C. A. Zificsak, 2001 .

Total syntheses of enantiomerically enriched R-(+)- and S-(-)-deplancheine.

R. Hsung, N. Sydorenko, A. Gerasyuto, 2005, Organic & biomolecular chemistry.

Synthesis of 2-(α-substituted-amidoalkyl)-imidazoles

D. Hlasta, C. A. Zificsak, 2005 .

A Rare Acid-Promoted Elimination of O-Methyl Oximes: A Practical Synthesis of 3-Cyano-4-benzopyrones

R. Hsung, Michelle B. Kim, Thuy-Trang T. Tran, 1999 .

A stereoselective intramolecular halo-etherification of chiral enamides in the synthesis of halogenated cyclic ethers.

Z. Al-Rashid, R. Hsung, Changhong Ko, 2007, Organic letters.

Stereoselective trans- and cis-dihydroxylations of 2H-pyranyl and dihydropyridinyl heterocycles synthesized from formal [3 + 3]-cycloaddition reactions of alpha,beta-unsaturated iminium ions with 1,3-dicarbonyl equivalents.

R. Hsung, K. P. Cole, M. McLaughlin, 2001, Organic letters.

Synthesis of dihydroxanthone derivatives and evaluation of their inhibitory activity against acetylcholinesterase: unique structural analogs of tacrine based on the BCD-ring of arisugacin.

R. Hsung, J. Mulder, G. Golding, 1999, Bioorganic & medicinal chemistry letters.

Highly stereoselective synthesis of novel alpha-haloenamides via a mild and efficient hydrohalogenation of ynamides.

R. Hsung, M. O. Frederick, J. Mulder, 2003, Organic letters.

Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone. A Highly Stereoselective Synthesis of Acrylic Acid Derivatives and 1,3-Dienes Using an Electron Deficient Variant of Ynamine

R. Hsung, J. Mulder, C. Douglas, 1999 .

The First Stereoselective Ficini—Claisen Rearrangement Using Chiral Ynamides.

R. Hsung, M. O. Frederick, J. Mulder, 2010 .

Synthesis and structure-activity relationships of 1,2,3,4-tetrahydropyrido[2,3-b]pyrazines as potent and selective inhibitors of the anaplastic lymphoma kinase.

A. Ghose, K. L. Milkiewicz, T. Underiner, 2010, Bioorganic & medicinal chemistry.

Strategies to mitigate the bioactivation of 2-anilino-7-aryl-pyrrolo[2,1-f][1,2,4]triazines: identification of orally bioavailable, efficacious ALK inhibitors.

K. Wells-Knecht, H. Breslin, B. Dorsey, 2012, Journal of medicinal chemistry.

Methanesulfonamido-cyclohexylamine derivatives of 2,4-diaminopyrimidine as potent ALK inhibitors.

T. Underiner, B. Dorsey, T. Angeles, 2011, Bioorganic & medicinal chemistry letters.

Optimization of a novel kinase inhibitor scaffold for the dual inhibition of JAK2 and FAK kinases.

Jennifer L. Mason, P. Dobrzanski, K. L. Milkiewicz, 2012, Bioorganic & medicinal chemistry letters.

Combined inhibition of atypical PKC and histone deacetylase 1 is cooperative in basal cell carcinoma treatment.

A. Butte, M. Sirota, S. Aasi, 2017, JCI insight.

Fused bicyclic derivatives of 2,4-diaminopyrimidine as c-Met inhibitors.

K. L. Milkiewicz, T. Underiner, B. Dorsey, 2011, Bioorganic & medicinal chemistry letters.

An Improved Synthesis of Canthin-6-one

Steven M. Mennen, Kevin M. Czerwinski, J. Stevens, 2003 .