Synthesis of aminophosphonate haptens for an aminoacylation reaction between methyl glucoside and a β-alanyl ester

Timo Lintunen, Jari Yli-Kauhaluoma (Corresponding Author)

Research output: Contribution to journalArticleScientificpeer-review

33 Citations (Scopus)

Abstract

Two 2-aminophosphonate haptens derived from methyl α-d-glucopyranoside were synthesized to mimic the transition-state of a transesterification reaction between methyl α-d-glucopyranoside and 4-nitrophenylester of tert-BOC-β-alanine. Two sets of monoclonal antibodies were generated against these haptens.

Original languageEnglish
Pages (from-to)1749-1750
JournalBioorganic and Medicinal Chemistry Letters
Volume10
Issue number15
DOIs
Publication statusPublished - 2000
MoE publication typeA1 Journal article-refereed

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