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Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes

Baldwin, Jack E., Adlington, Robert M., Lowe, Christopher, O'Neil, Ian A., Sanders, Gillian L., Schofield, Christopher J. and Sweeney, Joseph B. (1988) Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes. Journal of the Chemical Society, Chemical Communications (15). p. 1030. ISSN 0022-4936
Abstract

Reaction of 2-bromo-N-benzoylglycine methyl ester with 2-functionalised allyl stannane reagents under radical conditions provides a new route to α-alkylated amino acids in good yield, as exemplified by the facile synthesis of 4-methylene glutamate

Information
URI:
https://eprints.hud.ac.uk/id/eprint/15422
URI:
https://eprints.hud.ac.uk/id/eprint/15422
URI:
https://eprints.hud.ac.uk/id/eprint/15422
URI:
https://eprints.hud.ac.uk/id/eprint/15422
Title:
Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanes
Creators:
Baldwin, Jack E., Adlington, Robert M., Lowe, Christopher, O'Neil, Ian A., Sanders, Gillian L., Schofield, Christopher J. and Sweeney, Joseph B.
Identification Number:
https://doi.org/10.1039/c39880001030
Official URL:
http://dx.doi.org/10.1039/c39880001030
Date:
January 1988
Subjects:
Q Science > QD Chemistry
Schools:
School of Applied Sciences
Library
Item Type:
Article
Depositing User:
Joseph Sweeney
Date Deposited:
09 Oct 2012 09:20
Revision:
10
Last Modified:
28 Aug 2021 11:22
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