Abstract
AMONG removable groups employed for protecting the amino group of amino-acids and peptides, the phthalyl group has the advantage of giving stable and easily crystallizable derivatives1–5. Splitting of such N-phthalyl groups is usually accomplished by refluxing with alcoholic hydrazine hydroxide, followed by heating with dilute aqueous acid2–5.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Billman, J. H., and Harting, W. F., J. Amer. Chem. Soc., 70, 1473 (1948).
Ing, H. R., and Manske, R. H. F., J. Chem. Soc., 2348 (1926).
Kidd, D. A., and King, F. E., Nature, 162, 776 (1948); J. Chem. Soc., 3315 (1949).
Sheehan, J. C., and Frank, V. S., J. Amer. Chem. Soc., 71, 1856 (1949).
Grassmann, W., and Schulte-Uebbing, E., Ber., 83, 244 (1950).
Dunlap, F. L., J. Amer. Chem. Soc., 27, 1099 (1905).
Scheiber, J., Ber., 46, 1103 (1913).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
SCHUMANN, I., BOISSONNAS, R. Splitting of N-phthalyl Groups of Amino-acids with Phenylhydrazine. Nature 169, 154–155 (1952). https://doi.org/10.1038/169154a0
Issue Date:
DOI: https://doi.org/10.1038/169154a0
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.