Convenient preparation of N-maleoyl amino acid succinimido esters using N-trifluoroacetoxysuccinimide

M J Paterson; I M Eggleston

doi:10.1080/00397910701750151

Convenient preparation of N-maleoyl amino acid succinimido esters using N-trifluoroacetoxysuccinimide

M J Paterson, I M Eggleston

Department of Life Sciences

Research output: Contribution to journal › Article › peer-review

15 Citations (SciVal)

Abstract

One-pot cyclization and esterification of readily available maleamic acid derivatives using N-trifluoroacetoxysuccinimide provide a convenient and cost-effective route to a variety of useful N-maleoyl amino acid N-hydroxysuccinimido esters.

Original language	English
Pages (from-to)	303-308
Number of pages	6
Journal	Synthetic Communications
Volume	38
Issue number	2
DOIs	https://doi.org/10.1080/00397910701750151
Publication status	Published - 2008

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ID number: ISI:000253042000020

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10.1080/00397910701750151

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title = "Convenient preparation of N-maleoyl amino acid succinimido esters using N-trifluoroacetoxysuccinimide",

abstract = "One-pot cyclization and esterification of readily available maleamic acid derivatives using N-trifluoroacetoxysuccinimide provide a convenient and cost-effective route to a variety of useful N-maleoyl amino acid N-hydroxysuccinimido esters.",

author = "Paterson, \{M J\} and Eggleston, \{I M\}",

note = "ID number: ISI:000253042000020",

year = "2008",

doi = "10.1080/00397910701750151",

language = "English",

volume = "38",

pages = "303--308",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor and Francis",

number = "2",

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T1 - Convenient preparation of N-maleoyl amino acid succinimido esters using N-trifluoroacetoxysuccinimide

AU - Paterson, M J

AU - Eggleston, I M

N1 - ID number: ISI:000253042000020

PY - 2008

Y1 - 2008

N2 - One-pot cyclization and esterification of readily available maleamic acid derivatives using N-trifluoroacetoxysuccinimide provide a convenient and cost-effective route to a variety of useful N-maleoyl amino acid N-hydroxysuccinimido esters.

AB - One-pot cyclization and esterification of readily available maleamic acid derivatives using N-trifluoroacetoxysuccinimide provide a convenient and cost-effective route to a variety of useful N-maleoyl amino acid N-hydroxysuccinimido esters.

UR - https://www.scopus.com/pages/publications/38349169662

UR - http://dx.doi.org/10.1080/00397910701750151

U2 - 10.1080/00397910701750151

DO - 10.1080/00397910701750151

M3 - Article

SN - 0039-7911

VL - 38

SP - 303

EP - 308

JO - Synthetic Communications

JF - Synthetic Communications

IS - 2

ER -

Convenient preparation of N-maleoyl amino acid succinimido esters using N-trifluoroacetoxysuccinimide

Abstract

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