Solution-phase synthesis of aminooxy peptoids in the C to N and N to C directions

Injae Shin, Kisoo Park

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

(equation presented) Aminooxy peptoids, which are potential peptidomimetics, were synthesized by a stepwise monomer assembly. Ns-protected N-substituted aminooxyacetate tert-butyl esters were used as a monomer in both the C to N and the N to C directions. Submonomer synthesis of aminooxy peptoids is also described.

Original languageEnglish
Pages (from-to)869-872
Number of pages4
JournalOrganic Letters
Volume4
Issue number6
DOIs
Publication statusPublished - 2002 Mar 21

Fingerprint

Peptoids
monomers
Monomers
Aminooxyacetic Acid
Peptidomimetics
synthesis
esters
Esters
assembly
Direction compound

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

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abstract = "(equation presented) Aminooxy peptoids, which are potential peptidomimetics, were synthesized by a stepwise monomer assembly. Ns-protected N-substituted aminooxyacetate tert-butyl esters were used as a monomer in both the C to N and the N to C directions. Submonomer synthesis of aminooxy peptoids is also described.",
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Solution-phase synthesis of aminooxy peptoids in the C to N and N to C directions. / Shin, Injae; Park, Kisoo.

In: Organic Letters, Vol. 4, No. 6, 21.03.2002, p. 869-872.

Research output: Contribution to journalArticle

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