150117-06-9Relevant academic research and scientific papers
Design and synthesis of a trifunctional chiral porphyrin with C2 symmetry as a chiral recognition host for amino acid esters
Mizutani, Tadashi,Ema, Tadashi,Tomita, Takashi,Kuroda, Yasuhisa,Ogoshi, Hisanobu
, p. 4240 - 4250 (2007/10/02)
An intrinsic chiral recognition host, (R,R)- or (S.S)-[trans-5,15-bis(2-hydroxyphenyl)-10-{2,6-bis((methoxycarbonyl)m ethyl)phenyl}-2,3,17,18-tetraethylporphyrinato]zinc(II) (1), was synthesized by the coupling between (3,3',4,4'-tetraethyl-5,5'-bis(α-hyd
Recognition of Chirality and Residual Groups of Amino Acid Esters using New Trifunctional Chiral Porphyrins with C2 Symmetry
Mizutani, Tadashi,Ema, Tadashi,Tomita, Takashi,Kuroda, Yasuhisa,Ogoshi, Hisanobu
, p. 520 - 522 (2007/10/02)
An intrinsic chiral recognition host, -2,3,17,18-tetraethylporphyrinato>zinc(II) 1, is synthesized and found to show an enantioselectivity of ca. 2:1 for L- and D-amino acid esters having non-polar residues, whereas it shows a reversed enantioselectivity of ca. 1:2 for L- and D-Ser-OBzl.
