Approaches to the synthesis of ureapeptoid peptidomimetics

DOI: 10.1016/S0040-4039(97)01166-0

Source and publish data:

Tetrahedron Letters p. 5335 - 5338 (1997)

Update date:2022-08-03

Topics:

Authors:

Kruijtzer, John A. W.

Lefeber, Dirk J.

Liskamp, Rob M. J.

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Article abstract of DOI:10.1016/S0040-4039(97)01166-0

Ureapeptoid peptidomimetics can be composed from Boc-protected N-substituted ethylenediamines. The best approach is to synthesize these from chloroacetonitrile followed by conversion to the corresponding crystalline p-nitrophenyl carbamates in order to prepare the ureapeptoids.

Full text of DOI:10.1016/S0040-4039(97)01166-0

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Product name:Acetonitrile, [[[4-(1,1-dimethylethoxy)phenyl]methyl]amino]-

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