|1.||Kim, Yong-Sun: 1 article (08/2009)|
|2.||Carp, Richard I: 1 article (08/2009)|
|3.||Choi, Eun-Kyoung: 1 article (08/2009)|
|4.||Kim, Jae-Il: 1 article (08/2009)|
|5.||Lee, Yun-Jung: 1 article (08/2009)|
|6.||Jeong, Byung-Hoon: 1 article (08/2009)|
|7.||Jin, Jae-Kwang: 1 article (08/2009)|
|8.||Choi, Jin-Kyu: 1 article (08/2009)|
|9.||Kim, Nam-Ho: 1 article (08/2009)|
|10.||Krossing, I: 1 article (01/2001)|
09/01/1967 - "The tumor lipid was subjected to saponification, transesterification, and lithium aluminum hydride reduction. "
12/01/1990 - "This component, the least hydrophobic of the tumor-localizing fraction, was deemed to be dihematoporphyrin ether, based on mass spectrometric analysis and its behavior toward base hydrolysis and lithium aluminum hydride reduction. "
09/01/1987 - "Probing the structure and stability of the tumor-localizing derivative of hematoporphyrin by reductive cleavage with LiAlH4."
09/01/1987 - "A procedure involving the use of the reducing agent lithium aluminum hydride (LiAlH4) has been designed to explore the nature of the oligomer linkages in the tumor-localizing component of hematoporphyrin derivative (HPD). "
|2.||Prion Diseases (Transmissible Spongiform Encephalopathies)
08/01/2009 - "Reduction of prion infectivity and levels of scrapie prion protein by lithium aluminum hydride: implications for RNA in prion diseases."
08/01/2009 - "Treatment with RNase A alone and PrP degradation by RNase A plus proteinase K in vitro, however, did not result in loss of scrapie infectivity compared with the effects of lithium aluminum hydride. "
08/01/2009 - "Lithium aluminum hydride, a reducing agent that can induce reductive cleavage of oxidized molecules such as carbonyls, carboxyl acids, esters, and phosphodiester bonds, did not affect cellular PrP degradation; however, it destroyed PrPSc, extended the scrapie incubation period, and markedly reduced total RNA concentrations. "
|4.||Contagious Ecthyma (Orf)
|5.||Dehydration (Water Stress)
02/01/1996 - "Addition of a series of perfluoroalkylorganometallic reagents (RFLi; RF = C2F5, C3F7, or C4F9) to the 3 position of silylated testosterone 2b afforded delta 4 perfluoroalkyl carbinols 3. In Scheme 1, deprotection with HF and oxidation at the C-17 carbon with PCC produced delta 4 ketones 5. In Scheme 2 dehydration of 3 with 1,2-phenylenephosphorochloridite and iodine afforded delta 3,5 dienes 6 which were deprotected and oxidized as above to the C-17 ketones 8. In Scheme 3 isomerization of the double bond of 3 from the C-4 to the C-5 position using the allylic halogenation followed by treatment with lithium aluminum hydride led to the synthesis of the double bond isomer series 12. "
|1.||lithium aluminum hydride
|2.||Endopeptidase K (Proteinase K)
|4.||Dihematoporphyrin Ether (Porfimer Sodium)
|6.||RNA (Ribonucleic Acid)
|7.||Pancreatic Ribonuclease (Ribonuclease A)
|10.||Indicators and Reagents (Reagents)