94427-23-3Relevant academic research and scientific papers
Intramolecular benzyl-benzyl interactions in protonated benzyl diethers in the gas phase. Effects of internal hydrogen bonding
Edelson-Averbukh, Marina,Etinger, Alexander,Mandelbaum, Asher
, p. 1095 - 1105 (2007/10/03)
Protonated molecules of a variety of benzyl diethers, produced by chemical ionization (CI), undergo a unique rearrangement yielding relatively abundant mlz 181 C14H13+ ions, both in the ion source and under collision-induc
Monobenzylation of 1,n-diols via dibutylstannylene intermediates
Mash, Eugene A.,Kantor, Liza T. A.,Waller, Stephen C.
, p. 507 - 514 (2007/10/03)
Symmetrical primary 1,n-diols, HO(CH2)(n)OH, of any chain length from n = 2-10, can be selectively monobenzylated via sequential treatment with dibutyltin oxide and benzyl bromide.
Inhibition of matrix metalloproteinases by hydroxamates containing heteroatom-based modifications of the P1' group
Gowravaram,Tomczuk,Johnson,Delecki,Cook,Ghose,Mathiowetz,Spurlino,Rubin,Smith,Pulvino,Wahl
, p. 2570 - 2581 (2007/10/02)
In this study, structure-based drug design of matrix metalloproteinase inhibitors [human fibroblast collagenase (HFC), human fibroblast stromelysin (HFS), and human neutrophil collagenase (HNC)] was utilized in the development of potent hydroxamates which
Novel Antitumor Agents CI-920, PD 113270 and PD 113271. 3. Structure Determination.
Hokanson, Gerard C.,French, James C.
, p. 462 - 466 (2007/10/02)
The chemical structures for the novel phosphate-containing antitumor agents CI-920 (1), PD 113270 (2), and PD 113271 (3) were determined by a combination of spectra and chemical means.Extensive analysis of NMR spectral data allowed tentative structures to be assigned for these compounds and their derivatives.These structures were confirmed by reducing CI-920 to 8-methyl-1-octadecanol and by cleaving dephosphorylated CI-920 (7) with sodium periodate to identified products.
