156558-06-4Relevant academic research and scientific papers
Stereoselective synthesis and thromboxane A2 (TXA2) receptor antagonistic activity of optically active phenol derivatives
Fukumoto, Shoji,Terashita, Zen-Ichi,Ashida, Yasuko,Terao, Shinji,Shiraishi, Mitsuru
, p. 749 - 755 (2007/10/03)
Enantiomers of four potent nonprostanoid thromboxane A2 (TXA2) receptor antagonists, (±)-7-(4-fluorophenyl)-7-(2-hydroxyphenyl)heptanoic acids (1- 4), were synthesized stereoselectively by direct ortho-alkylation of phenols under mod
Direct and enantiospecific ortho-benzylation of phenols by the Mitsunobu reaction
Fukumoto, Shoji,Fukushi, Shigeha,Terao, Shinji,Shiraishi, Mitsuru
, p. 1021 - 1026 (2007/10/03)
ortho-Substituted phenol derivatives with high optical purity have been obtained directly by Mitsunobu reaction between an appropriate phenol and an optically active benzyl alcohol. In this reaction, the chemical yield was well balanced with the optical p
Optically active phenol derivatives and preparation thereof
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, (2008/06/13)
An optically active tri-substituted methane compound having, as substituents, an aromatic ring group and a phenyl group having hydroxyl group at ortho or para position can be obtained by allowing a phenol compound unsubstituted at the ortho- or/and para-p
