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

doi:10.1016/0040-4039(84)80112-4

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 journal › Article › peer-review

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 language	English
Pages (from-to)	3711-3714
Number of pages	4
Journal	Tetrahedron Letters
Volume	25
Issue number	34
DOIs	https://doi.org/10.1016/0040-4039(84)80112-4
Publication status	Published - 1984
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/0040-4039(84)80112-4

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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.",

author = "Kahee Fujita and Seiji Ejima and Tadashi Ueda and Taiji Imoto and Schulten, {Hans Rolf}",

year = "1984",

doi = "10.1016/0040-4039(84)80112-4",

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AU - Fujita, Kahee

AU - Ejima, Seiji

AU - Ueda, Tadashi

AU - Imoto, Taiji

AU - Schulten, Hans Rolf

PY - 1984

Y1 - 1984

N2 - 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.

AB - 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.

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U2 - 10.1016/0040-4039(84)80112-4

DO - 10.1016/0040-4039(84)80112-4

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