S. Miller

发表

Development of a practical synthesis of novel, pyrrole-based HMG-CoA reductase inhibitors

J. Pfefferkorn, Chulho Choi, Yun-Song Song, 2007 .

Rationalization of the unusual electrochemical behavior observed in lariat ethers and other reducible macrocyclic systems

D. A. Gustowski, G. Gokel, A. Kaifer, 1988 .

Synthesis of pyrimidine analogs of 2,6‐Di‐tert‐butylphenol antiinflammatory agents

D. T. Connor, P. Unangst, C. Kostlan, 1995 .

Synthesis and structure-activity relationship of 2-amino-3-heteroaryl-quinoxalines as non-peptide, small-molecule antagonists for interleukin-8 receptor.

D. T. Connor, B. Roth, S. Qin, 2003, Bioorganic & medicinal chemistry.

Design and synthesis of hepatoselective, pyrrole-based HMG-CoA reductase inhibitors.

G. Lu, J. Pfefferkorn, M. Harris, 2007, Bioorganic & medicinal chemistry letters.

DETECTION OF ULTRA-TRACE LEVELS OF URANIUM IN AQUEOUS SAMPLES BY LASER INDUCED FLUORESCENCE SPECTROMETRY

T. Hirschfeld, F. Milanovich, D. Perry, 1981 .

One-pot conversion of alkynes and alkenes into one-carbon homologated aldehydes via hydrozirconation-isocyanide insertion-hydrolysis

E. Negishi, D. Swanson, S. Miller, 1988 .

Stereoselective synthesis of exocyclic alkenes via zirconium-promoted alkyl-diene coupling

E. Negishi, S. Miller, 1989 .

Solid-state structural chemistry of lariat ether and BiBLE cation complexes: metal-ion identity and coordination number determine cavity size

V. J. Gatto, G. Gokel, C. Minganti, 1986 .

Tribracchial lariat ethers, ‘TriBLEs,’ based on 4,10,16-triaza-18-crown-6: an apparent limit to sidearm contributions in lariat ether molecules

G. Gokel, T. P. Cleary, F. Fronczek, 1989 .

Syntheses and binding properties of bibrachial lariat ethers (BiBLEs): survey of synthetic methods and cation selectivities

V. J. Gatto, G. Gokel, C. R. Morgan, 1986 .

Novel synthetic access to 15- and 18-membered ring diaza-bibracchial lariat ethers (BiBLEs) and a study of sidearm-macroring cooperativity in cation binding

V. J. Gatto, G. Gokel, K. Arnold, 1986 .

Neutral lonophores having extraordinary Ca2+ binding strengths and Ca2+/Na+ selectivities in aqueous solution

C. Li, O. Schall, A. Nakano, 1990 .

Hepatoselectivity of statins: design and synthesis of 4-sulfamoyl pyrroles as HMG-CoA reductase inhibitors.

Yuntao Song, Bruce Auerbach, Lisa Dillon, 2008, Bioorganic & medicinal chemistry letters.

Steroidal lariat ethers: a new class of macrocycles and the crystal structure of N-(cholesteryloxycarbonyl)aza-15-crown-5

G. Gokel, L. Echegoyen, C. Minganti, 1987 .

(1S, 3S)-3-amino-4-difluoromethylenyl-1-cyclopentanoic acid (CPP-115), a potent γ-aminobutyric acid aminotransferase inactivator for the treatment of cocaine addiction.

J. Brodie, A. Schousboe, C. Craft, 2012, Journal of medicinal chemistry.

Synthesis of novel 5-hydroxy-3-alkoxy- and 5-hydroxy-3-alkylthioindole-2-carboxamides

D. T. Connor, P. Unangst, S. Miller, 1996 .

Synthesis of Novel 5-Hydroxy-3-alkoxy- and 5-Hydroxy-3-alkylthioindole- 2-carboxamides.

D. T. Connor, P. Unangst, S. Miller, 1997 .

(1S, 3S)-3-amino-4-difluoromethylenyl-1-cyclopentanoic acid (CPP-115), a potent γ-aminobutyric acid aminotransferase inactivator for the treatment of cocaine addiction.

J. Brodie, A. Schousboe, C. Craft, 2012, Journal of medicinal chemistry.

Synthesis of novel 3‐alkoxy‐ and 3‐alkylthioindole and ‐benzofuran‐2‐carboxamides

P. Unangst, S. Miller, D. Connor, 1996 .