J. Sabol

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Recent Advances in the Synthesis of Piperidones and Piperidines

J. Kane, P. Weintraub, J. Sabol, 2003 .

A new method for the electrophilic fluorination of vinyl stannanes

D. Matthews, J. Mccarthy, J. Sabol, 1993 .

MDL 28,753, an agonist of LTD4 but an antagonist of LTC4 in longitudinal muscle of guinea pig ileum.

J. Sabol, R. Raddatz, T. Gieske, 1990, The Journal of pharmacology and experimental therapeutics.

Terminal fluoroolefins. The synthesis of novel carboacyclic nucleosides.

J. Mccarthy, J. Sabol, S. Miller, 1998, Nucleosides & nucleotides.

Constrained amino acids. An approach to the synthesis of 3-substituted prolines

E. Huber, J. Sabol, G. Flynn, 1996 .

A stereocontrolled approach to substituted piperidones and piperidines: flavopiridol D-ring analogs

D. Friedrich, J. Sabol, D. Borcherding, 2001 .

Recent Advances in the Synthesis of Piperidones and Piperidines

J. Kane, P. Weintraub, J. Sabol, 2003 .

Synthesis and SAR of novel 4,5-diarylimidazolines as potent P2X7 receptor antagonists.

D. Rampe, P. Shum, J. Sabol, 2005, Bioorganic & medicinal chemistry letters.

Conformationally restricted leukotriene antagonists. Asymmetric synthesis of some nor-leukotriene D4 analogs

R. J. Cregge, J. Sabol, 1989 .

Conformationally restricted leukotriene antagonists. Synthesis of some leukotriene D4 analogs from D-xylose

R. J. Cregge, J. Sabol, 1989 .

CONSTRAINED AMINO ACIDS. THE SYNTHESIS OF GLUTAMINE MIMETICS

D. Friedrich, E. Huber, J. Sabol, 1997 .

A new route to 1,1-difluoro olefins: Application to the synthesis of 2′-deoxy-2′-difluoromethylene nucleosides.

J. Mccarthy, J. Sabol, 1992 .

A nonbleachable rhodopsin analogue formed from 11, 12-dihydroretinal.

K. Nakanishi, M. Gawinowicz, J. Sabol, 1977, Journal of the American Chemical Society.

Improved Synthesis of (E)-2′-Deoxy-2′-(fluoromethylene)cytidine - A Potent Inhibitor Of Ribonucleotide Diphosphate Reductase

D. Matthews, J. Mccarthy, J. Sabol, 1993 .

Syntheses of -2-fluoromethy--tyrosine and -2-difluoromethyl--tyrosine as potential inhibitors of tyrosine hydroxylase

I. McDonald, J. Sabol, M. Jung, 1991 .

Inhibition of myeloperoxidase release from rat polymorphonuclear leukocytes by a series of azachalcone derivatives.

M. L. Edwards, D. Stemerick, R. Dinerstein, 1994, Journal of medicinal chemistry.

Design of a Fluoro-olefin Cytidine Nucleoside as a Bioprecursor of a Mechanism-Based Inhibitor of Ribonucleotide Reductase

A. Bitonti, J. Stubbe, P. Sunkara, 1996 .

Conformationally restricted leukotriene antagonists. Asymmetric synthesis of a nor-leokotriene D4 analog. II.

R. J. Cregge, J. Sabol, 1990 .

The synthesis of (1-fluorovinyl)tributyltin: A synthetic equivalent for the 1-fluoroethene anion

D. Matthews, J. Mccarthy, J. Sabol, 1994 .