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

32 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
Number of pages2
JournalBioorganic and Medicinal Chemistry Letters
Volume10
Issue number15
DOIs
Publication statusPublished - 2000
MoE publication typeA1 Journal article-refereed

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Aminoacylation
Haptens
Glucosides
Esters
Transesterification
Alanine
Monoclonal Antibodies

Cite this

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title = "Synthesis of aminophosphonate haptens for an aminoacylation reaction between methyl glucoside and a β-alanyl ester",
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.",
author = "Timo Lintunen and Jari Yli-Kauhaluoma",
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Synthesis of aminophosphonate haptens for an aminoacylation reaction between methyl glucoside and a β-alanyl ester. / Lintunen, Timo; Yli-Kauhaluoma, Jari (Corresponding Author).

In: Bioorganic and Medicinal Chemistry Letters, Vol. 10, No. 15, 2000, p. 1749 - 1750.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - Synthesis of aminophosphonate haptens for an aminoacylation reaction between methyl glucoside and a β-alanyl ester

AU - Lintunen, Timo

AU - Yli-Kauhaluoma, Jari

N1 - Project code: K7SU00342

PY - 2000

Y1 - 2000

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AB - 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.

U2 - 10.1016/S0960-894X(00)00328-0

DO - 10.1016/S0960-894X(00)00328-0

M3 - Article

VL - 10

SP - 1749

EP - 1750

JO - Bioorganic and Medicinal Chemistry Letters

JF - Bioorganic and Medicinal Chemistry Letters

SN - 0960-894X

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ER -