B. A. Hathaway

发表

Synthesis, structure, electrostatic properties and spectroscopy of 3-methyl-4,5,6,7-tetrafluoro-1H-indazole. An experimental and ab initio computational study†

G. Day, R. Glaser, M. R. Lewis, 1998 .

An aldol condensation experiment using a number of aldehydes and ketones

B. A. Hathaway, 1987 .

Comparison of Iodination of Methoxylated Benzaldehydes and Related Compounds using Iodine/Silver Nitrate and Iodine/Periodic Acid

B. A. Hathaway, Kristen L. White, Mark E. McGill, 2007 .

4‐Methoxybenzaldehyde pentafluorophenylmethylidenehydrazone

C. Barnes, R. Glaser, B. A. Hathaway, 1999 .

Selective Preparation of 4-(Bromo or Iodo)-2,5-dimethoxybenzonitrile and 2-(Bromo or Iodo)-3,6-dimethoxybenzonitrile from 2,5-Dimethoxybenzaldehyde

J. Wittenborn, B. A. Hathaway, Brian E. Taylor, 1998 .

Organic Chemistry, Sixth Edition (Solomons, T.W. Graham)

B. A. Hathaway, 1992 .

Comparison of solution conformational preferences for the hallucinogens bufotenin and psilocin using 360-MHz proton NMR spectroscopy.

G. Migliaccio, S. Byrn, T. Shieh, 1981, Journal of medicinal chemistry.

Selective Preparation of 4‐(Bromo or Iodo)‐2,5‐dimethoxybenzonitrile and 2‐(Bromo or Iodo)‐3,6‐dimethoxybenzonitrile from 2,5‐Dimethoxybenzaldehyde.

J. Wittenborn, B. A. Hathaway, Brian E. Taylor, 1999 .

1,2-Diiodo-4,5-dimethylbenzene

Uriah J. Kilgore, M. Bond, B. A. Hathaway, 2009, Acta crystallographica. Section E, Structure reports online.

Inhibition of human dihydrofolate reductase by 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-(substituted-phenyl)-s-triazine s. A quantitative structure-activity relationship analysis.

C. Hansch, J. Freisheim, Z. Guo, 1984, Journal of medicinal chemistry.

Crystallography, quantitative structure-activity relationships, and molecular graphics in a comparative analysis of the inhibition of dihydrofolate reductase from chicken liver and Lactobacillus casei by 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-(substituted-phenyl)-s-triazine s.

R. Langridge, C. Hansch, J. Blaney, 1984, Journal of medicinal chemistry.