Zobrazeno 1 - 10
of 15
pro vyhledávání: '"James B. Springer"'
Publikováno v:
The Journal of organic chemistry. 64(14)
New photochemically removable protecting groups have been developed based on classical nitrobenzyl compounds modified by the inclusion of a pentadienyl group. It serves to trap through an internal Diels-Alder reaction the nitroso group produced as pa
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 57:110-114
The prodrugs cyclophosphamide (CP) and ifosfamide (IF) each metabolize to an active alkylating agent through a cytochrome P450-mediated oxidation at the C-4 position. Competing with this activation pathway are enzymatic oxidations at the exocyclic α
Autor:
Michael P. Gamcsik, Rebecca L. Mutesi, Michael A. D'Alessandro, James B. Springer, Prince N. A. Amoyaw, Collin R. Dempsey, Susan M. Ludeman
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 54:607-612
Effects of neurodegeneration have been linked to inefficient detoxification of free radicals due to lowered concentrations of antioxidants, especially glutathione, in the brain. In the biosynthesis of glutathione, cysteine concentration is generally
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 50:115-122
A variety of deuterated 3-amino-1-propanols were made by the LiAlD 4 or AlD 3 reduction of nitrile or ester precursors. The labeled aminopropanols and/or deuterated bis(2-chloroethyl)amines were used to synthesize [4,4- 2 H 2 ]-, [6,6- 2 H 2 ]-, [α,
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 50:79-84
Reduction of diethyliminodiacetate with [ 3 H]-LiAlH 4 and then reaction with SOCl 2 gave bis(2-chloro-2-[ 3 H] ethyl)amine hydrochloride. This compound, together with [ 33 P]-phosphorus oxychloride, provided for the synthesis of [ 3 H, 33 P]-phospho
Autor:
Susan M. Ludeman, Mihir C. Gandhi, M. Eileen Dolan, Sonali M. Smith, Lynette R. Wilson, James B. Springer
Publikováno v:
Cancer Chemotherapy and Pharmacology. 52:291-302
O6-benzylguanine (BG) is a unique purine analog that has been shown to influence nitrogen mustard activity and increase cytotoxicity. Ifosfamide is a nitrogen mustard with growing clinical applications; effective modulation may lead to improved effic
Autor:
Michael P. Gamcsik, Kai-Liu Shao, Susan M. Ludeman, O. Michael Colvin, David J. Adams, James B. Springer, Jila H. Boal, James L. Flowers
Publikováno v:
Cancer Chemotherapy and Pharmacology. 45:335-344
A number of investigators have observed that the use of 4-hydroperoxycyclophosphamide (4-HC) in multiwell plate cytotoxicity assays can be associated with toxicity to cells in wells that contain no drug. Previous reports have implicated diffusion of
Publikováno v:
Journal of labelled compoundsradiopharmaceuticals. 57(2)
The prodrugs cyclophosphamide (CP) and ifosfamide (IF) each metabolize to an active alkylating agent through a cytochrome P450-mediated oxidation at the C-4 position. Competing with this activation pathway are enzymatic oxidations at the exocyclic α
Publikováno v:
The Journal of Organic Chemistry. 61:1436-1442
In order to determine the reactive geometries of enone−TiCl4 complexes in Diels−Alder reactions compounds 1a·TiCl4 and 1b·TiCl4 were prepared. A crystal structure of 1a·TiCl4 confirmed that the titanium in this complex has the desired out-of-p
Autor:
Robert C. Corcoran, James B. Springer
Publikováno v:
The Journal of Organic Chemistry. 61:1443-1448
Reaction of diastereomeric β-benzyloxy enones with TiCl4 results in the cleavage of the benzyl ethers and yields substrates for Diels−Alder reactions which incorporate covalently attached Lewis acids. The axial CH2OTiCl3 group of 2a unambiguously