M. E. Flaugh

发表

Inhibition of luteinizing hormone release and ovulation by 6-chloro- and 6-fluoromelatonin.

J. Clemens, B. Sawyer, J. Parli, 1980, Neuroendocrinology.

Preparation of 8-Amido-2-dimethylamino-1,2,3,4-tetrahydro-2-dibenzofurans and several fluorinated derivatives via [3,3]-sigmatropic rearrangement of O-aryloximes.

Sean R. Dinn, A. Kiefer, Steven W. Tregay, 2003, The Journal of organic chemistry.

TWO EFFICIENT SYNTHESES OF INDOLE-3-PROPIONIC ESTERS AND ACIDS. FURTHER APPLICATIONS OF MELDRUM'S ACID

M. E. Flaugh, D. Farlow, P. Pranc, 1981 .

Acid-catalyzed annelation of .alpha.-alkylaldehydes and .alpha.,.beta.-unsaturated ketones. A one-pot synthesis of 4,4-dimethyl-2-cyclohexen-1-one

M. E. Flaugh, D. Farlow, T. Crowell, 1980 .

6-substituted 1,3,4,5-tetrahydrobenz[cd]indol-4-amines: potent serotonin agonists.

R. Fuller, N. Mason, D. Mullen, 1988, Journal of medicinal chemistry.

Synthesis of porphyrins. Deoxophylloerythroetioporphyrin

H. Rapoport, M. E. Flaugh, 1968 .

Synthesis and evaluation of the antiovulatory activity of a variety of melatonin analogues.

J. Clemens, B. Sawyer, M. E. Flaugh, 1979, Journal of medicinal chemistry.

ACID‐CATALYZED ANNELATION OF α‐ALKYLALDEHYDES AND α,β‐UNSATURATED KETONES. A ONE‐POT SYNTHESIS OF 4,4‐DIMETHYL‐2‐CYCLOHEXEN‐1‐ONE

M. E. Flaugh, D. Farlow, T. Crowell, 1981 .

Characterization of LY344864 as a pharmacological tool to study 5-HT1F receptors: binding affinities, brain penetration and activity in the neurogenic dural inflammation model of migraine.

T. Branchek, J. Zgombick, P. Gilbert, 1997, Life sciences.

5‐HT1F receptor agonists inhibit neurogenic dural inflammation in guinea pigs

Kirk W. Johnson, T. Branchek, J. Zgombick, 1997, Neuroreport.

Preclinical studies on LY228729: a potent and selective serotonin1A agonist.

D. Wong, R. Fuller, D. Nelson, 1993, The Journal of pharmacology and experimental therapeutics.

Pharmacological characterization of LY293284: A 5-HT1A receptor agonist with high potency and selectivity.

R. Fuller, D. Nelson, K. Rasmussen, 1994, The Journal of pharmacology and experimental therapeutics.

Preparation of 8-Amido-2-dimethylamino-1,2,3,4-tetrahydro-2-dibenzofurans and several fluorinated derivatives via [3,3]-sigmatropic rearrangement of O-aryloximes.

Sean R. Dinn, A. Kiefer, Steven W. Tregay, 2003, The Journal of organic chemistry.