A facile synthesis of NZ/Boc-protected 1, 3, 4-oxadiazole-based peptidomimetics employing peptidyl thiosemicarbazides
RS Lamani, G Nagendra, VV Sureshbabu
Index: Lamani, Ravi S.; Nagendra; Sureshbabu, Vommina V. Tetrahedron Letters, 2010 , vol. 51, # 36 p. 4705 - 4709
Full Text: HTML
Citation Number: 14
Abstract
Synthesis of 1, 3, 4-oxadiazole containing peptidomimetics is described by a p-TsCl/pyridine- mediated cyclization of the corresponding dipeptidyl thiosemicarbazides, which are readily prepared by coupling N-protected amino acid hydrazides with amino acid-derived isothiocyanato esters. Further, the protocol has also been extended for the synthesis of orthogonally protected 1, 3, 4-oxadiazole tethered mimetics as well. The synthetic route is ...
Related Articles:
[Michalski, Oskar; Ciez, Dariusz Journal of Molecular Structure, 2013 , vol. 1037, p. 225 - 235]
SYNTHESIS OF CHIRAL THIOCARBAMOYLPHOSPHINES DERIVED FROM AMINO ACIDS1
[Kunze, U.; Burghardt, R. Phosphorus and Sulfur and the Related Elements, 1987 , vol. 29, p. 373 - 376]