Isoselenocyanates derived from Boc/Z-amino acids: synthesis, isolation,characterization, and application to the efficient synthesis of unsymmetrical selenoureas and selenoureidopeptidomimetics


Autoria(s): Chennakrishnareddy, Gundala; Nagendra, Govindappa; Hemantha, Hosahalli P; Das, Ushati; Row, Tayur Guru N; Sureshbabu, Vommina V
Data(s)

21/08/2010

Resumo

Isoselenocyanates derived from Boc/Z-amino acids are prepared by the reaction of the corresponding isonitriles with selenium powder in presence of triethylamine at reflux. The utility of these new classes of isoselenocyanates in the preparation of selenoureidodipeptidomimetics possessing both amino as well as carboxy termini has been accomplished. The H-1 NMR analysis confirmed that the protocol involving the conversion of isonitriles to isoselenocyanates and their use as coupling agents in assembling selenour-eido derivatives is free from racemization. (C) 2010 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/32014/1/derived.pdf

Chennakrishnareddy, Gundala and Nagendra, Govindappa and Hemantha, Hosahalli P and Das, Ushati and Row, Tayur Guru N and Sureshbabu, Vommina V (2010) Isoselenocyanates derived from Boc/Z-amino acids: synthesis, isolation,characterization, and application to the efficient synthesis of unsymmetrical selenoureas and selenoureidopeptidomimetics. In: Tetrahedron, 66 (34). pp. 6718-6724.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/j.tet.2010.06.082

http://eprints.iisc.ernet.in/32014/

Palavras-Chave #Solid State & Structural Chemistry Unit
Tipo

Journal Article

PeerReviewed