Synthesis of a C20-Deoxygenated Spirangien Derivative for Target Identification

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

Organisationseinheiten

Externe Organisationen

  • Helmholtz-Zentrum für Infektionsforschung GmbH (HZI)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)797-801
Seitenumfang5
FachzeitschriftSYNLETT
Jahrgang26
Ausgabenummer6
PublikationsstatusVeröffentlicht - 2015

Abstract

The synthesis of a C20-deoxygenated spirangien derivative is described that allows the incorporation of various affinity labels for target identification of this potent natural product. The synthesis takes advantage of two major building blocks that can be accessed in 8 and 14 steps, respectively. The endgame joins both fragments through a selective aldol reaction and final protecting group manipulations furnish the target molecule.

ASJC Scopus Sachgebiete

Zitieren

Synthesis of a C20-Deoxygenated Spirangien Derivative for Target Identification. / Bluhm, Nadine; Kalesse, Markus.
in: SYNLETT, Jahrgang 26, Nr. 6, 2015, S. 797-801.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Download
@article{e6fc22c534904290af79d2f0086831f8,
title = "Synthesis of a C20-Deoxygenated Spirangien Derivative for Target Identification",
abstract = "The synthesis of a C20-deoxygenated spirangien derivative is described that allows the incorporation of various affinity labels for target identification of this potent natural product. The synthesis takes advantage of two major building blocks that can be accessed in 8 and 14 steps, respectively. The endgame joins both fragments through a selective aldol reaction and final protecting group manipulations furnish the target molecule.",
keywords = "aldol reaction, natural product synthesis, spirangien, target identification",
author = "Nadine Bluhm and Markus Kalesse",
note = "Publisher Copyright: {\textcopyright} Georg Thieme Verlag.",
year = "2015",
doi = "10.1055/s-0034-1379980",
language = "English",
volume = "26",
pages = "797--801",
journal = "SYNLETT",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "6",

}

Download

TY - JOUR

T1 - Synthesis of a C20-Deoxygenated Spirangien Derivative for Target Identification

AU - Bluhm, Nadine

AU - Kalesse, Markus

N1 - Publisher Copyright: © Georg Thieme Verlag.

PY - 2015

Y1 - 2015

N2 - The synthesis of a C20-deoxygenated spirangien derivative is described that allows the incorporation of various affinity labels for target identification of this potent natural product. The synthesis takes advantage of two major building blocks that can be accessed in 8 and 14 steps, respectively. The endgame joins both fragments through a selective aldol reaction and final protecting group manipulations furnish the target molecule.

AB - The synthesis of a C20-deoxygenated spirangien derivative is described that allows the incorporation of various affinity labels for target identification of this potent natural product. The synthesis takes advantage of two major building blocks that can be accessed in 8 and 14 steps, respectively. The endgame joins both fragments through a selective aldol reaction and final protecting group manipulations furnish the target molecule.

KW - aldol reaction

KW - natural product synthesis

KW - spirangien

KW - target identification

UR - http://www.scopus.com/inward/record.url?scp=84925493612&partnerID=8YFLogxK

U2 - 10.1055/s-0034-1379980

DO - 10.1055/s-0034-1379980

M3 - Article

AN - SCOPUS:84925493612

VL - 26

SP - 797

EP - 801

JO - SYNLETT

JF - SYNLETT

SN - 0936-5214

IS - 6

ER -

Von denselben Autoren