Hexafluoroacetone as protecting and activating reagent: An efficient strategy for activation of pyroglutamic acid and homologues

Ksenia Pumpor; Christoph Böttcher; Susanna Fehn; Klaus Burger

doi:10.3987/com-03-s34

Hexafluoroacetone as protecting and activating reagent: An efficient strategy for activation of pyroglutamic acid and homologues

Ksenia Pumpor, Christoph Böttcher, Susanna Fehn, Klaus Burger^*

^*Korrespondierende/r Autor/-in für diese Arbeit

Institut für Biochemie

Universität Leipzig

9 Zitate (Scopus)

Abstract

Hexafluoroacetone-protected glutamic acid on treatment with thionyl chloride is transformed into a carboxy-activated pyroglutamic acid derivative. Likewise, the reaction sequence can be applied to aminoadipic acid and homologues.

Originalsprache	Englisch
Zeitschrift	Heterocycles
Jahrgang	61
Seiten (von - bis)	259-269
Seitenumfang	11
ISSN	0385-5414
DOIs	https://doi.org/10.3987/com-03-s34
Publikationsstatus	Veröffentlicht - 31.12.2003

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

Dokumente

10.3987/com-03-s34

Weitere Links

Link to publication in Scopus

Zitieren

@article{a3441584988e4020bcb394bf015e74b3,

title = "Hexafluoroacetone as protecting and activating reagent: An efficient strategy for activation of pyroglutamic acid and homologues",

abstract = "Hexafluoroacetone-protected glutamic acid on treatment with thionyl chloride is transformed into a carboxy-activated pyroglutamic acid derivative. Likewise, the reaction sequence can be applied to aminoadipic acid and homologues.",

author = "Ksenia Pumpor and Christoph B{\"o}ttcher and Susanna Fehn and Klaus Burger",

year = "2003",

month = dec,

day = "31",

doi = "10.3987/com-03-s34",

language = "English",

volume = "61",

pages = "259--269",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

}

TY - JOUR

T1 - Hexafluoroacetone as protecting and activating reagent: An efficient strategy for activation of pyroglutamic acid and homologues

AU - Pumpor, Ksenia

AU - Böttcher, Christoph

AU - Fehn, Susanna

AU - Burger, Klaus

PY - 2003/12/31

Y1 - 2003/12/31

N2 - Hexafluoroacetone-protected glutamic acid on treatment with thionyl chloride is transformed into a carboxy-activated pyroglutamic acid derivative. Likewise, the reaction sequence can be applied to aminoadipic acid and homologues.

AB - Hexafluoroacetone-protected glutamic acid on treatment with thionyl chloride is transformed into a carboxy-activated pyroglutamic acid derivative. Likewise, the reaction sequence can be applied to aminoadipic acid and homologues.

UR - https://www.scopus.com/pages/publications/0347022244

U2 - 10.3987/com-03-s34

DO - 10.3987/com-03-s34

M3 - Journal articles

AN - SCOPUS:0347022244

SN - 0385-5414

VL - 61

SP - 259

EP - 269

JO - Heterocycles

JF - Heterocycles

ER -

Hexafluoroacetone as protecting and activating reagent: An efficient strategy for activation of pyroglutamic acid and homologues

Abstract

UN SDGs

Strategische Forschungsbereiche und Zentren

Dokumente

Weitere Links

Fingerprint

Zitieren