896-32-2Relevant articles and documents
2,2,2-Triphenylethanol: a Hydrogen-Bonded Tetramer Based upon a Centrosymmetric R44(8) Motif
Ferguson, George,Glidewell, Christopher,Zakaria, Choudhury M.
, p. 928 - 931 (1994)
2,2,2-Triphenylethanol, C20H18O, crystallizes as hydrogen-bonded tetrameric aggregates which are centrosymmetric.The resulting planar O4 ring is almost square with O...O distances of 2.786(2) and 2.822(2) Angstroem; the hydroxyl H atoms are fully ordered,
First selective CYP11B1 inhibitors for the treatment of cortisol-dependent diseases
Hille, Ulrike E.,Zimmer, Christina,Vock, Carsten A.,Hartmann, Rolf W.
supporting information; experimental part, p. 2 - 6 (2011/04/17)
Outgoing from an etomidate-based design concept, we succeeded in the development of a series of highly active and selective inhibitors of CYP11B1, the key enzyme of cortisol biosynthesis, as potential drugs for the treatment of Cushing's syndrome and rela
Enantioselective TADMAP-catalyzed carboxyl migration reactions for the synthesis of stereogenic quaternary carbon
Shaw, Scott A.,Aleman, Pedro,Christy, Justin,Kampf, Jeff W.,Va, Porino,Vedejs, Edwin
, p. 925 - 934 (2007/10/03)
The chiral, nucleophilic catalyst TADMAP [1, 3-(2,2,2-triphenyl-1- acetoxyethyl)-4-(dimethylamino)-pyridine] has been prepared from 3-lithio-4-(dimethylamino)pyridine (5) and triphenylacetaldehyde (3), followed by acylation and resolution. TADMAP catalyzes the carboxyl migration of oxazolyl, furanyl, and benzofuranyl enol carbonates with good to excellent levels of enantioselection. The oxazole reactions are especially efficient and are used to prepare chiral lactams (23) and lactones (30) containing a quaternary asymmetric carbon. TADMAP-catalyzed carboxyl migrations in the indole series are relatively slow and proceed with inconsistent enantioselectivity. Modeling studies (B3LYP/6-31G*) have been used in qualitative correlations of catalyst conformation, reactivity, and enantioselectivity.
