Difference in orientation of a guest within a cavity of β-cyclodextrins bearing an N-acetylaminoacyl group

Iwao Suzuki, Ryoko Onodera, Jun Ichi Anzai

Research output: Contribution to journalArticlepeer-review

Abstract

1H-NMR studies revealed that either the benzene or the naphthalene ring of 8-anilinonaphthalene-1-sulfonate (ANS) was accommodated by β-cyclodextrin (β-CyD) bearing an N-Ac-L-Leu residue, while β-CyDs bearing an N-Ac-L-Ile and N-Ac-L-Val residues accommodated the naphthalene ring of ANS.

Original languageEnglish
Pages (from-to)567-570
Number of pages4
JournalHeterocycles
Volume52
Issue number2
DOIs
Publication statusPublished - 2000 Feb 1

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Difference in orientation of a guest within a cavity of β-cyclodextrins bearing an N-acetylaminoacyl group'. Together they form a unique fingerprint.

Cite this