67246-78-0Relevant academic research and scientific papers
Enantioresolution of 2-methoxy-2-(1-naphtyl)propionic acid using diastereomeric salt formation with chiral phenylethylamine
Kusakari, Miho,Ohta, Yurie,Nakagawa, Hideaki,Katagiri, Hiroshi,Kijima, Tatsuro,Murakami, Satoshi,Matsuba, Shigeru,Hatano, Bunpei
, p. 4114 - 4116 (2014)
An enantioresolution of 2-methoxy-2-(1-naphtyl)propionic acid (MαNP acid) using the diastereomeric salt with chiral (R)-phenylethylamine was achieved to give enantiopure (R)-MαNP acid in 29% yield with >99% ee based on rac-MαNP acid. X-ray crystallographi
Crystal structures and chiral recognition of the diastereomeric salts prepared from 2-methoxy-2-(1-naphthyl)propanoic acid
Ichikawa, Akio,Ono, Hiroshi,Echigo, Takuya,Mikata, Yuji
experimental part, p. 4536 - 4548 (2012/05/20)
This paper is the first to report the structures of crystalline diastereomeric salts 8 and 9 prepared from (R)-2-methoxy-2-(1-naphthyl)propanoic acid [(R)-MαNP acid, (R)-1] and (S)-1 with (R)-1-phenylethylamine [(R)-PEA, (R)-7], respectively. These crysta
