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

Timo Lintunen; Jari Yli-Kauhaluoma

doi:10.1016/S0960-894X(00)00328-0

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

Timo Lintunen
, Jari Yli-Kauhaluoma^*

^*Corresponding author for this work

VTT Technical Research Centre of Finland

Research output: Contribution to journal › Article › Scientific › peer-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 language	English
Pages (from-to)	1749-1750
Journal	Bioorganic and Medicinal Chemistry Letters
Volume	10
Issue number	15
DOIs	https://doi.org/10.1016/S0960-894X(00)00328-0
Publication status	Published - 2000
MoE publication type	A1 Journal article-refereed

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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",

note = "Project code: K7SU00342",

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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

N2 - 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.

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

SN - 0960-894X

VL - 10

SP - 1749

EP - 1750

JO - Bioorganic and Medicinal Chemistry Letters

JF - Bioorganic and Medicinal Chemistry Letters

IS - 15

ER -

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

Abstract

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