Single step syntheses of ω-9-fluorenylmethyl esters of aspartic and glutamic acids

Article abstract of DOI:10.1080/00397919208019289

Base lability of the 9-fluorenylmethyl ester makes this group useful in solid phase peptide synthesis when used in combination with the tBoc methodology for preparing cyclic peptides. We describe a simple one step synthesis of the 9-fluorenylmethyl esters of aspartic and glutamic acids.

Full text of DOI:10.1080/00397919208019289

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Single Step Syntheses of ω-9-
Fluorenylmethyl Esters of
Aspartic and Glutamic Acids
Peter J. Belshaw a , J. Gordon Adamson a & Gilles A.
Lajoie a
a Department of Chemistry , University of Waterloo ,
Waterloo, Ont., Canada , N2L 3G1
Published online: 24 Sep 2006.
To cite this article: Peter J. Belshaw , J. Gordon Adamson & Gilles A. Lajoie (1992)
Single Step Syntheses of ω-9-Fluorenylmethyl Esters of Aspartic and Glutamic Acids,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 22:7, 1001-1005, DOI: 10.1080/00397919208019289
To link to this article: http://dx.doi.org/10.1080/00397919208019289
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