Meta/para-selectivity variation by sulfide/sulfoxide conversion of 6-substituted β-cyclodextrin. Hydrolyses of nitrophenyl acetates. ag

Kahee Fujita, Seiji Ejima, Tadashi Ueda, Taiji Imoto, Hans Rolf Schulten

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Hydrolyses of m- and p-nitrophenyl acetates by 6-deoxy-6-alkylthio-β-cyclodextrins and the corresponding sulfoxides were studied to show that the small chemical conversion from the sulfides to the sulfoxides led to a change of meta/para-selectivity in the hydrolysis of the β-cyclodextrin moiety.

Original languageEnglish
Pages (from-to)3711-3714
Number of pages4
JournalTetrahedron Letters
Volume25
Issue number34
DOIs
Publication statusPublished - 1984
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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