Highly diastereoselective radical reactions of substituted methylideneimidazolidinones and related systems

George A. Adamson; Athelstan L.J. Beckwith; Christina L.L. Chai

doi:10.1071/CH04054

Highly diastereoselective radical reactions of substituted methylideneimidazolidinones and related systems

George A. Adamson, Athelstan L.J. Beckwith^*, Christina L.L. Chai

^*Corresponding author for this work

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

9 Citations (Scopus)

Abstract

Stannane-mediated radical addition to tnethylideneimidazolidinones occurs with good to excellent diastereo-selectivity. The stereochemical outcome of addition is highly dependent on the nature of the NI substituent on the imidazolidinone ring.

Original language	English
Pages (from-to)	629-633
Number of pages	5
Journal	Australian Journal of Chemistry
Volume	57
Issue number	7
DOIs	https://doi.org/10.1071/CH04054
Publication status	Published - 2004

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@article{37f946938470468ca9848a69e3a93c4b,

title = "Highly diastereoselective radical reactions of substituted methylideneimidazolidinones and related systems",

abstract = "Stannane-mediated radical addition to tnethylideneimidazolidinones occurs with good to excellent diastereo-selectivity. The stereochemical outcome of addition is highly dependent on the nature of the NI substituent on the imidazolidinone ring.",

author = "Adamson, {George A.} and Beckwith, {Athelstan L.J.} and Chai, {Christina L.L.}",

year = "2004",

doi = "10.1071/CH04054",

language = "English",

volume = "57",

pages = "629--633",

journal = "Australian Journal of Chemistry",

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publisher = "CSIRO",

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T1 - Highly diastereoselective radical reactions of substituted methylideneimidazolidinones and related systems

AU - Adamson, George A.

AU - Beckwith, Athelstan L.J.

AU - Chai, Christina L.L.

PY - 2004

Y1 - 2004

N2 - Stannane-mediated radical addition to tnethylideneimidazolidinones occurs with good to excellent diastereo-selectivity. The stereochemical outcome of addition is highly dependent on the nature of the NI substituent on the imidazolidinone ring.

AB - Stannane-mediated radical addition to tnethylideneimidazolidinones occurs with good to excellent diastereo-selectivity. The stereochemical outcome of addition is highly dependent on the nature of the NI substituent on the imidazolidinone ring.

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U2 - 10.1071/CH04054

DO - 10.1071/CH04054

M3 - Article

SN - 0004-9425

VL - 57

SP - 629

EP - 633

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

IS - 7

ER -

Highly diastereoselective radical reactions of substituted methylideneimidazolidinones and related systems

Abstract

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