Syntheses and crystal structures of 4,5-dihydro-2-(2-hydroxyphenyl)oxazole-containing metal complexes was written by Bolm, Carsten; Weickhardt, Konrad; Zehnder, Margareta; Glasmacher, Dorothea. And the article was included in Helvetica Chimica Acta on June 19,1991.Formula: C13H17NO2 The following contents are mentioned in the article:
ML2 (M = Cu, HL = I (R = H, R1 = CHMe2, Ph, CMe3 or R = Ph, RI = Me); M = Zn, Co, Ni, FeCl, R = H, R1 = CHMe2) and I were prepared ML2 (M = Cu, Zn, Ni; R = H, R1 = CHMe2) were analyzed by x-ray diffraction studies [monoclinic, space group P21, A2, A2, Z = 4, 2, 2, Rw = 0.078, 0.074, 0.060, resp.]. L coordinates through the hydrooxazole N and phenolato O atoms. CuL2 and NiL2 have a distorted square planar configuration whereas ZnL2 has a distorted tetrahedral configuration. ML2 were characterized by IR and mass spectra. This study involved multiple reactions and reactants, such as (S)-2-(4-(tert-Butyl)-4,5-dihydrooxazol-2-yl)phenol (cas: 135948-04-8Formula: C13H17NO2).
(S)-2-(4-(tert-Butyl)-4,5-dihydrooxazol-2-yl)phenol (cas: 135948-04-8) belongs to oxazolidine derivatives. Oxazolidine-based compounds are well-known chiral auxiliaries and strategic molecular moieties in chemistry since they can effectively mask or mimic amino acid units or amino alcohols. Some reports highlighted again the effectiveness of oxazolidine-based compounds in driving the stereo- or diastereotopic outcome of chemical reactions.Formula: C13H17NO2
135948-04-8;(S)-2-(4-(tert-Butyl)-4,5-dihydrooxazol-2-yl)phenol;The future of 135948-04-8;New trend of C13H17NO2;function of 135948-04-8