Sesquiterpene Backbones Generated by Sesquiterpene Cyclases: Formation of iso-Caryolan-1-ol and an Isoclovane

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

Organisationseinheiten

Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)8575-8579
Seitenumfang5
FachzeitschriftOrganic letters
Jahrgang25
Ausgabenummer48
Frühes Online-Datum27 Nov. 2023
PublikationsstatusVeröffentlicht - 8 Dez. 2023

Abstract

New sesquiterpene backbones are accessible after incubation of caryolan-synthase (GcoA) and presilphiperfolan-8-β-ol synthase (BcBOT2) with a non-natural farnesyldiphosphate in which the central olefinic double bond is isomerized toward the methyl group. Two newly formed sesquiterpenoids are reported, a constitutional isomer of caryolan-1-ol (3), which we name iso-caryolan-1-ol (17), and the first terpenoid based on the isoclovane ring skeleton generated enzymatically thus far.

ASJC Scopus Sachgebiete

Zitieren

Sesquiterpene Backbones Generated by Sesquiterpene Cyclases: Formation of iso-Caryolan-1-ol and an Isoclovane. / Struwe, Henry; Schrödter, Finn; Spinck, Hanke et al.
in: Organic letters, Jahrgang 25, Nr. 48, 08.12.2023, S. 8575-8579.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Struwe H, Schrödter F, Spinck H, Kirschning A. Sesquiterpene Backbones Generated by Sesquiterpene Cyclases: Formation of iso-Caryolan-1-ol and an Isoclovane. Organic letters. 2023 Dez 8;25(48):8575-8579. Epub 2023 Nov 27. doi: 10.1021/acs.orglett.3c03383
Struwe, Henry ; Schrödter, Finn ; Spinck, Hanke et al. / Sesquiterpene Backbones Generated by Sesquiterpene Cyclases : Formation of iso-Caryolan-1-ol and an Isoclovane. in: Organic letters. 2023 ; Jahrgang 25, Nr. 48. S. 8575-8579.
Download
@article{271af95d6edf436bac5bb10af005d4a7,
title = "Sesquiterpene Backbones Generated by Sesquiterpene Cyclases: Formation of iso-Caryolan-1-ol and an Isoclovane",
abstract = "New sesquiterpene backbones are accessible after incubation of caryolan-synthase (GcoA) and presilphiperfolan-8-β-ol synthase (BcBOT2) with a non-natural farnesyldiphosphate in which the central olefinic double bond is isomerized toward the methyl group. Two newly formed sesquiterpenoids are reported, a constitutional isomer of caryolan-1-ol (3), which we name iso-caryolan-1-ol (17), and the first terpenoid based on the isoclovane ring skeleton generated enzymatically thus far.",
author = "Henry Struwe and Finn Schr{\"o}dter and Hanke Spinck and Andreas Kirschning",
note = "Funding information: We thank Dr. J{\"o}rn Droste (Leibniz University Hannover) for expert support in all issues concerning NMR spectroscopic analysis.",
year = "2023",
month = dec,
day = "8",
doi = "10.1021/acs.orglett.3c03383",
language = "English",
volume = "25",
pages = "8575--8579",
journal = "Organic letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "48",

}

Download

TY - JOUR

T1 - Sesquiterpene Backbones Generated by Sesquiterpene Cyclases

T2 - Formation of iso-Caryolan-1-ol and an Isoclovane

AU - Struwe, Henry

AU - Schrödter, Finn

AU - Spinck, Hanke

AU - Kirschning, Andreas

N1 - Funding information: We thank Dr. Jörn Droste (Leibniz University Hannover) for expert support in all issues concerning NMR spectroscopic analysis.

PY - 2023/12/8

Y1 - 2023/12/8

N2 - New sesquiterpene backbones are accessible after incubation of caryolan-synthase (GcoA) and presilphiperfolan-8-β-ol synthase (BcBOT2) with a non-natural farnesyldiphosphate in which the central olefinic double bond is isomerized toward the methyl group. Two newly formed sesquiterpenoids are reported, a constitutional isomer of caryolan-1-ol (3), which we name iso-caryolan-1-ol (17), and the first terpenoid based on the isoclovane ring skeleton generated enzymatically thus far.

AB - New sesquiterpene backbones are accessible after incubation of caryolan-synthase (GcoA) and presilphiperfolan-8-β-ol synthase (BcBOT2) with a non-natural farnesyldiphosphate in which the central olefinic double bond is isomerized toward the methyl group. Two newly formed sesquiterpenoids are reported, a constitutional isomer of caryolan-1-ol (3), which we name iso-caryolan-1-ol (17), and the first terpenoid based on the isoclovane ring skeleton generated enzymatically thus far.

UR - http://www.scopus.com/inward/record.url?scp=85179612914&partnerID=8YFLogxK

U2 - 10.1021/acs.orglett.3c03383

DO - 10.1021/acs.orglett.3c03383

M3 - Article

C2 - 38011332

AN - SCOPUS:85179612914

VL - 25

SP - 8575

EP - 8579

JO - Organic letters

JF - Organic letters

SN - 1523-7060

IS - 48

ER -

Von denselben Autoren