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 language | English |
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Pages (from-to) | 3711-3714 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 25 |
Issue number | 34 |
DOIs | |
Publication status | Published - 1984 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry