Synthesis of orthogonally protected vicinal diamines with amino acid-based skeleton
Publication type: Journal Article
Publication date: 2002-01-01
SJR: —
CiteScore: —
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ISSN: 09295666, 1573496X
Biochemistry
Abstract
A convenient route to amino acid-based orthogonally protected 1,2-diamines starting from materials readily available for a peptide chemist is presented. The key step of the procedure is the Mitsunobu reaction of N-protected aminoalcohol, obtained by the reduction of commercially available Z- or Boc-protected amino acid, with imidodicarbonate or sulfonylcarbamate related to standard amino-protecting groups used in peptide chemistry yielding triprotected vicinal diamines.
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Juszczyk P. Synthesis of orthogonally protected vicinal diamines with amino acid-based skeleton // Letters in Peptide Science. 2002. Vol. 9. No. 4. pp. 187-192.
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Juszczyk P. Synthesis of orthogonally protected vicinal diamines with amino acid-based skeleton // Letters in Peptide Science. 2002. Vol. 9. No. 4. pp. 187-192.
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RIS
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TY - JOUR
DO - 10.1023/a:1024127015979
UR - https://doi.org/10.1023/a:1024127015979
TI - Synthesis of orthogonally protected vicinal diamines with amino acid-based skeleton
T2 - Letters in Peptide Science
AU - Juszczyk, Paulina
PY - 2002
DA - 2002/01/01
PB - Springer Nature
SP - 187-192
IS - 4
VL - 9
SN - 0929-5666
SN - 1573-496X
ER -
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@article{2002_Juszczyk,
author = {Paulina Juszczyk},
title = {Synthesis of orthogonally protected vicinal diamines with amino acid-based skeleton},
journal = {Letters in Peptide Science},
year = {2002},
volume = {9},
publisher = {Springer Nature},
month = {jan},
url = {https://doi.org/10.1023/a:1024127015979},
number = {4},
pages = {187--192},
doi = {10.1023/a:1024127015979}
}
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MLA
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Juszczyk, Paulina. “Synthesis of orthogonally protected vicinal diamines with amino acid-based skeleton.” Letters in Peptide Science, vol. 9, no. 4, Jan. 2002, pp. 187-192. https://doi.org/10.1023/a:1024127015979.