Application of the C3-Methyltransferase StspM1 for the Synthesis of the Natural Pyrroloindole Motif-Reference-Cited by-同舟云学术

Application of the C3-Methyltransferase StspM1 for the Synthesis of the Natural Pyrroloindole Motif

Published:2023-12-14 Issue:1 Volume:14 Page:227-236
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Haase Mona¹,David Benoit²,Paschold Beatrix¹,Classen Thomas³^ORCID,Schneider Pascal¹,Pozhydaieva Nadiia¹^ORCID,Gohlke Holger²⁴^ORCID,Pietruszka Jörg¹³^ORCID

Affiliation:

1. Institute for Bioorganic Chemistry & Bioeconomy Science Center (BioSC), Heinrich Heine University Düsseldorf in Forschungszentrum Jülich, 52426 Jülich, Germany

2. Institute of Bio- and Geosciences (IBG-4: Bioinformatics) Forschungszentrum Jülich, 52426 Jülich, Germany

3. Institute of Bio- and Geosciences (IBG-1: Bioorganic Chemistry) & Bioeconomy Science Center (BioSC), Forschungszentrum Jülich, 52426 Jülich, Germany

4. Institute for Pharmaceutical and Medicinal Chemistry & Bioeconomy Science Center (BioSC), Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany

Funder

European Regional Development Fund

Forschungszentrum J?lich

Heinrich-Heine-Universit?t D?sseldorf

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.3c04952

Reference35 articles.

1. 2,5-Diketopiperazines: Synthesis, Reactions, Medicinal Chemistry, and Bioactive Natural Products

2. Chaetocin: a promising new antimyeloma agent with in vitro and in vivo activity mediated via imposition of oxidative stress

3. Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis

4. Biocatalytic C3‐Indole Methylation—A Useful Tool for the Natural‐Product‐Inspired Stereoselective Synthesis of Pyrroloindoles

5. Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters

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