Zobrazeno 1 - 10 of 10 pro vyhledávání: '"T. E. Levitt"'
2
Radioimmunoassay of lysergic acid diethylamide (LSD) in serum and urine by using antisera of different specificities
Autor: W. A. Ratcliffe, W. A. Harland, T E Levitt, S M Fletcher, A C Moffat, J. G. Ratcliffe
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
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3
Experimental evaluation of paracetamol antidotes
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
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5
Radioimmunoassay of lysergic acid diethylamide (LSD) in serum and urine by using antisera of different specificities
Autor: W A, Ratcliffe, S M, Fletcher, A C, Moffat, J G, Ratcliffe, W A, Harland, T E, Levitt
Publikováno v: Clinical chemistry. 23(2 PT. 1)
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=pmid________::bae6cbe295520b01b7015d1a92bff5d2
https://pubmed.ncbi.nlm.nih.gov/832379
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7
Trismonoalkylaminoboranes in Organic Synthesis: the Exploitation of a New Type of ‘Activated Ester’
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
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9
Possible pathways for the reduction of carboxylic acids by diborane; the reductions of carboxylic and mixed anhydrides
Autor: Michael G. Hutchings, Keith Smith, T. E. Levitt, Andrew Pelter
Publikováno v: Journal of the Chemical Society D: Chemical Communications. :347
Two new reactions have been defined in the interactions of diborane with carboxylic acids: probable pathways of reduction of various acids are indicated, that of benzoic acid being very solvent sensitive.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::354daf005f8febd93bb9fc7526fadf0b
https://doi.org/10.1039/c29700000347
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10
Asymmetry associated with a borate salt
Autor: Andrew Pelter, T. E. Levitt
Publikováno v: Journal of the Chemical Society D: Chemical Communications. :1027a
A salt of the type XB-Y3Z+ exhibits asymmetry that may be ascribed to stereospecific ion-pairing.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a91708835afcb1fb7c12e058ed1a3007
https://doi.org/10.1039/c2969001027a
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