A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one

R Green; A T Merritt; S D Bull

doi:10.1039/b713966g

A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one

R Green, A T Merritt, S D Bull

Department of Chemistry

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

3 Citations (SciVal)

Abstract

A cleavable linker strategy has been used to optimise the enolate alkylation reactions of a recyclable L-tyrosine derived polymer-supported oxazolidin-2-one for the asymmetric synthesis of a series of chiral alpha-alkyl acids.

Original language	English
Pages (from-to)	508-510
Number of pages	3
Journal	Chemical Communications
Volume	4
DOIs	https://doi.org/10.1039/b713966g
Publication status	Published - 2008

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ID number: ISI:000252254500027

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title = "A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one",

abstract = "A cleavable linker strategy has been used to optimise the enolate alkylation reactions of a recyclable L-tyrosine derived polymer-supported oxazolidin-2-one for the asymmetric synthesis of a series of chiral alpha-alkyl acids.",

author = "R Green and Merritt, {A T} and Bull, {S D}",

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doi = "10.1039/b713966g",

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journal = "Chemical Communications",

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AU - Merritt, A T

AU - Bull, S D

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PY - 2008

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AB - A cleavable linker strategy has been used to optimise the enolate alkylation reactions of a recyclable L-tyrosine derived polymer-supported oxazolidin-2-one for the asymmetric synthesis of a series of chiral alpha-alkyl acids.

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UR - http://dx.doi.org/10.1039/b713966g

U2 - 10.1039/b713966g

DO - 10.1039/b713966g

M3 - Article

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EP - 510

JO - Chemical Communications

JF - Chemical Communications

ER -

A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one

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