Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones

F J P Feuillet; D G Niyadurupola; R Green; M Cheeseman; S D Bull

doi:10.1055/s-2005-865212

Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones

F J P Feuillet
, D G Niyadurupola
, R Green
, M Cheeseman
, S D Bull

Department of Chemistry

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

13 Citations (SciVal)

Abstract

Zinc alkoxides of syn- or anti-β-hydroxy-N-acyloxazolidin-2-ones undergo stereoselective rearrangement to afford their corresponding syn- or anti-N-2-hydroxyethyl-1,3-oxaziliane-2,4-diones in good yield.

Original language	English
Pages (from-to)	1090-1094
Number of pages	5
Journal	Synlett
Issue number	7
DOIs	https://doi.org/10.1055/s-2005-865212
Publication status	Published - 2005

Bibliographical note

ID number: ISI:000228951700003

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title = "Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones",

abstract = "Zinc alkoxides of syn- or anti-β-hydroxy-N-acyloxazolidin-2-ones undergo stereoselective rearrangement to afford their corresponding syn- or anti-N-2-hydroxyethyl-1,3-oxaziliane-2,4-diones in good yield.",

author = "Feuillet, \{F J P\} and Niyadurupola, \{D G\} and R Green and M Cheeseman and Bull, \{S D\}",

note = "ID number: ISI:000228951700003",

year = "2005",

doi = "10.1055/s-2005-865212",

language = "English",

pages = "1090--1094",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "7",

}

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T1 - Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones

AU - Feuillet, F J P

AU - Niyadurupola, D G

AU - Green, R

AU - Cheeseman, M

AU - Bull, S D

N1 - ID number: ISI:000228951700003

PY - 2005

Y1 - 2005

N2 - Zinc alkoxides of syn- or anti-β-hydroxy-N-acyloxazolidin-2-ones undergo stereoselective rearrangement to afford their corresponding syn- or anti-N-2-hydroxyethyl-1,3-oxaziliane-2,4-diones in good yield.

AB - Zinc alkoxides of syn- or anti-β-hydroxy-N-acyloxazolidin-2-ones undergo stereoselective rearrangement to afford their corresponding syn- or anti-N-2-hydroxyethyl-1,3-oxaziliane-2,4-diones in good yield.

U2 - 10.1055/s-2005-865212

DO - 10.1055/s-2005-865212

M3 - Article

SN - 0936-5214

SP - 1090

EP - 1094

JO - Synlett

JF - Synlett

IS - 7

ER -

Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones

Abstract

Bibliographical note

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