Recognition of planar chirality by cyclodextrins

Koji Kano, Ryoko Takaoka, Masayuki Sato, Masahiko Yamaguchi

Research output: Contribution to journalArticlepeer-review

Abstract

Recognition of planar chirality of 14-hydroxy-12-oxabicyclo[9.2.2]pentadecane-1 (14), 11(15)-diene-1,13-dione (C8) and 16-hydroxy-14-oxabicyclo[11.2.2]heptadecane-1(16),13(17)-diene-2,15-dione (C10) by native and O-methylated cyclodextrins has been studied by NMR spectroscopy. The cyclodextrins prefer the (R)-enantiomers of C8 and C10, which might well fit with asymmetrically twisted cavities of cyclodextrins.

Original languageEnglish
Pages (from-to)1337-1338
Number of pages2
JournalChemistry Letters
Issue number12
DOIs
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Chemistry(all)

Fingerprint Dive into the research topics of 'Recognition of planar chirality by cyclodextrins'. Together they form a unique fingerprint.

Cite this