1334208-34-2Relevant academic research and scientific papers
Hydrogen Bonds-Enabled Design of a C1-Symmetric Chiral Br?nsted Acid Catalyst
Momiyama, Norie,Funayama, Kosuke,Noda, Hirofumi,Yamanaka, Masahiro,Akasaka, Naohiko,Ishida, Shintaro,Iwamoto, Takeaki,Terada, Masahiro
, p. 949 - 956 (2016/02/18)
We have developed new C1-symmetric, chiral bis-phosphoric acids with an electron-withdrawing group as one of the two substituents. This C1-symmetric, chiral bis-phosphoric acid with a pentafluorophenyl group performs exceptionally we
BIS-PHOSPHATE COMPOUND AND ASYMMETRIC REACTION USING THE SAME
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Page/Page column 25, (2013/02/28)
A novel bis-phosphate compound is provided which can be applied to a wide range of reactive substrates and reactions as an asymmetric reaction catalyst and can realize an asymmetric reaction affording a high yield and a high enantiomeric excess. The bis-p
Design of chiral bis-phosphoric acid catalyst derived from (R)-3,3′-Di(2-hydroxy-3-arylphenyl)binaphthol: Catalytic enantioselective Diels-Alder reaction of α,β-unsaturated aldehydes with amidodienes
Momiyama, Norie,Konno, Tohru,Furiya, Yuichi,Iwamoto, Takeaki,Terada, Masahiro
supporting information; experimental part, p. 19294 - 19297 (2012/01/15)
Chiral bis-phosphoric acid 1 was designed to identify a new class of structural features in chiral Bronsted acid catalysts. X-ray diffraction analysis revealed the single atropisomer 1, bearing S axial chirality at 3,3′-biaryl substituents on (R)-binaphth
Bis-phosphoric acid derived from BINOL dimer as a chiral br?nsted acid catalyst for enantioselective transformations
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, (2019/03/08)
A chiral bis-phosphoric acid derived from a BINOL (1,1¤-bi-2-naphthol) dimer as a chiral backbone was developed. The catalytic efficiency of this bis-phosphoric acid was compared with that of a reported bis-phosphoric acid having a single BINOL backbone i
