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3684266 
Journal Article 
New submonomers for poly N-substituted glycines (peptoids) 
Uno, T; Beausoleil, E; Goldsmith, RA; Levine, BH; Zuckermann, RN 
1999 
1 
Tetrahedron Letters
ISSN: 0040-4039
EISSN: 1873-3581 
Elsevier 
Tetrahedron Letters 
40 
8 
1475-1478 
WOS:000078513400014 
Abstract: Five protected submonomers for peptoid synthesis were prepared, including N(in)-BOC-tryptamine, O-t-butyl tyramine, PMC-guanidino-propylamine, 6-amino-6-deoxy-D-galactopyranose diacetonide, and 5-amino-2,2-dimethyl-1,3-dioxane. The first three mimic natural aminoacid sidechains i.e, tryptophan, tyrosine, and arginine, while the last two provide hydrophilic sidechains. These submonomers were successfully used for preparation of oligo-peptoids by the submonomer synthesis method. (C) 1999 Elsevier Science Ltd. All rights reserved. ds: Chemistry cument Delivery No.: 165GU e field[29]: 1,4-Dioxane