Zobrazeno 1 - 10
of 86
pro vyhledávání: '"T. E. Levitt"'
Autor:
M. E. Rose, Julian Tyson, Michael L. Hitchman, E. J. Newman, James N. Miller, G. P. R. Carr, Joe P. Foley, R. D. McDowall, Elizabeth F. Hounsell, R. J. Flanagan, T. E. Levitt
Publikováno v:
The Analyst. 119:25N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e84e751016674ed7152ecec5a6c00d2
https://doi.org/10.1039/an994190025n
https://doi.org/10.1039/an994190025n
Publikováno v:
Clinical Chemistry. 23:169-174
We raised high-titre antisera to two LSD-bovine serum albumin conjugates, one linked via the indole nitrogen, the other via the amide side-chain. The antisera were specific for different parts of the LSD molecule, as demonstrated by cross-reactivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::711f1c17dbd3bda58da19343251e16aa
https://doi.org/10.1093/clinchem/23.2.169
https://doi.org/10.1093/clinchem/23.2.169
Publikováno v:
Chemical Communications; 7/4/2024, Vol. 60 Issue 52, p6671-6674, 4p
Autor:
Fuegen, Kathleen, Hatchett, Gregory T.
Publikováno v:
Teaching of Psychology; Jul2024, Vol. 51 Issue 3, p334-344, 11p
Autor:
F D Harvey, T E Levitt
Publikováno v:
The Journal of international medical research. 4
Introduction Recent work has suggested (Mitchell et al 1973a, Jollow et al 1973, Potter et al 1973, Mitchell et al 1973b, Mitchell et al 1974, Jollow et al 1974) that paracetamol* is partially converted in the liver to a reactive metabolite which is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a013ca57e8019e9fe9b73288cf9a797c
https://pubmed.ncbi.nlm.nih.gov/193746
https://pubmed.ncbi.nlm.nih.gov/193746
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac8fe072dce30df6f325857eea385cb7
https://doi.org/10.1002/chin.197745171
https://doi.org/10.1002/chin.197745171
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7c6e82da06e327c33bac91c60e1e6a8
https://doi.org/10.1002/chin.197024162
https://doi.org/10.1002/chin.197024162
Autor:
Bigelow, Taylor M.1 tbigelow@newhaven.edu, Das, Bagmi2, Gilfillan, Beth H.3, Forziat-Pytel, Kellie4,5, Galván, Angélica6, Kim, So Rin7
Publikováno v:
Journal of Creativity in Mental Health. Oct-Dec2022, Vol. 17 Issue 4, p502-517. 16p.
Autor:
Hatchett, Gregory T.1 (AUTHOR) hatchettg@nku.edu, Ripley, Dana1 (AUTHOR), Fuegen, Kathleen2 (AUTHOR)
Publikováno v:
Counselor Education & Supervision. Sep2022, Vol. 61 Issue 3, p217-229. 13p. 1 Chart.
Autor:
Andrew Pelter, T. E. Levitt
Publikováno v:
Nature. 211:299-300
WE have recently introduced the trisdialkylaminoboranes as new reagents for the synthesis of enamines and tertiary amides1. Similarly, the trismonoalkylaminoboranes react with ketones to yield Schiff's bases, and with carboxylic acids to give seconda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b54484056645c44fc8eaef9ddbde9742
https://doi.org/10.1038/211299a0
https://doi.org/10.1038/211299a0