T. Schaaf

发表

Direct effects of morphine but not of fentanyl‐type opioids on human 5‐HT3A receptors in outside‐out patch‐clamp studies

B. Urban, M. Wittmann, M. Lyutenska, 2014, European journal of pain.

Stereo-controlled synthesis of dl-prostaglandins F2.alpha. and E2

E. Corey, T. Schaaf, N. Weinshenker, 1969 .

Chapter 19. Modulation of the Arachidonic Acid Cascade

T. Schaaf, 1977 .

Chapter 9: Prostaglandin Structure-Activity Relationships

T. Schaaf, 1976 .

The Effects of Fentanyl-Like Opioids and Hydromorphone on Human 5-HT3A Receptors

B. Urban, M. Wittmann, M. Barann, 2008, Anesthesia and analgesia.

The Effects of Morphine on Human 5-HT3A Receptors

B. Urban, J. Nadstawek, M. Wittmann, 2006, Anesthesia and analgesia.

Radioimmunoassay for sulprostone.

T. Carty, T. Schaaf, F. Falkner, 1982, Prostaglandins, leukotrienes, and medicine.

New reagents for stereoselective carbonyl reduction. An improved synthetic route to the primary prostaglandins.

E. Corey, R. Varma, T. Schaaf, 1971, Journal of the American Chemical Society.

Stereospecific total synthesis of prostaglandins E3 and F3 alpha.

E. Corey, S. Terashima, H. Shirahama, 1971, Journal of the American Chemical Society.

Total synthesis of prostaglandins F1-alpha, E1, F2-alpha, and E2 (natural forms) from a common synthetic intermediate.

E. Corey, T. Schaaf, R. Nyori, 1970, Journal of the American Chemical Society.

Total synthesis of prostaglandins F2-alpha and E2 as the naturally occurring forms.

E. Corey, T. Schaaf, N. Weinshenker, 1970, Journal of the American Chemical Society.

Synthesis of 11.alpha.,9.alpha.-epoxymethanothromboxane A2: a stable, optically active TxA2 agonist

E. Corey, M. Parry, D. L. Bussolotti, 1981 .

Synthetic furocoumarins. IX. New synthetic route to psoralen

K. D. Kaufman, T. Schaaf, J. A. Weis, 1969 .

Synthetic modification of a novel microbial ionophore: exploration of anticoccidial structure-activity relationships.

T. Schaaf, A. P. Ricketts, J. Olson, 1992, Journal of medicinal chemistry.

Synthesis of tritium-labeled N-acetyl PGE2 carboxamide (CP-27,987).

T. Schaaf, 1979, Prostaglandins.

Total synthesis of prostaglandins F1.alpha. and E1

E. Corey, T. Schaaf, 1972 .

Structure activity studies leading to a tissue-selective hypotensive prostaglandin analog, 13,14-dihydro-16-phenyl-ω-tetranor PGE2

M. Johnson, T. Schaaf, J. W. Constantine, 1980 .

N-(Methanesulfonyl)-16-phenoxyprostaglandincarboxamides: tissue-selective, uterine stimulants.

M. Johnson, J. Plattner, J. Bindra, 1981, Journal of medicinal chemistry.

New extensions of the bicyclo[2.2.1]heptane route to prostaglandins.

E. Corey, J. Bindra, A. Grodski, 1973, Journal of the American Chemical Society.

Structure-activity studies of configurationally rigid arylprostaglandins.

M. Johnson, J. Bindra, T. Schaaf, 1983, Journal of medicinal chemistry.

Synthesis and biological activity of carboxyl-terminus modified prostaglandin analogues.

H. J. Hess, T. Schaaf, 1979, Journal of medicinal chemistry.

Stereo-controlled synthesis of prostaglandins F-2a and E-2 (dl).

E. Corey, T. Schaaf, N. Weinshenker, 1969, Journal of the American Chemical Society.

Benzodifurans. I. The synthesis of benzo[1,2‐b:5,4‐b]difuran and some methyl analogs

A. W. Burgstahler, K. D. Kaufman, T. Schaaf, 1969 .

Direct effects of morphine but not of fentanyl‐type opioids on human 5‐HT3A receptors in outside‐out patch‐clamp studies

B. Urban, M. Wittmann, M. Lyutenska, 2014, European journal of pain.