Anionic ring-contraction reaction of cyclic acetal system: Stereoselective approach to multi-functionalized oxetanes

Masaki Suzuki; Katsuhiko Tomooka

doi:10.1055/s-2004-817772

Anionic ring-contraction reaction of cyclic acetal system: Stereoselective approach to multi-functionalized oxetanes

Masaki Suzuki, Katsuhiko Tomooka

Research output: Contribution to journal › Article › peer-review

9 Citations (Scopus)

Abstract

The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.

Original language	English
Pages (from-to)	651-654
Number of pages	4
Journal	Synlett
Issue number	4
DOIs	https://doi.org/10.1055/s-2004-817772
Publication status	Published - Mar 9 2004
Externally published	Yes

All Science Journal Classification (ASJC) codes

Organic Chemistry

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title = "Anionic ring-contraction reaction of cyclic acetal system: Stereoselective approach to multi-functionalized oxetanes",

abstract = "The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.",

author = "Masaki Suzuki and Katsuhiko Tomooka",

year = "2004",

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doi = "10.1055/s-2004-817772",

language = "English",

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journal = "Synlett",

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AU - Tomooka, Katsuhiko

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AB - The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.

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DO - 10.1055/s-2004-817772

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SN - 0936-5214

IS - 4

ER -

Anionic ring-contraction reaction of cyclic acetal system: Stereoselective approach to multi-functionalized oxetanes

Abstract

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