Atroposelective Nenitzescu Indole Synthesis.


Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
02 May 2023
Historique:
medline: 24 3 2023
pubmed: 24 3 2023
entrez: 23 3 2023
Statut: ppublish

Résumé

Invited for the cover of this issue is the group of Frederic W. Patureau at the RWTH Aachen University. The image depicts atropoisomerism, in particular through the helix-shaped vines in the forefront focus. This metaphorically illustrates the importance of atroposelectivity in biologically active molecules, such as in the 5-hydroxyindoles that were accessed through the first enantioselective Nenitzescu indole synthesis. Read the full text of the article at 10.1002/chem.202300279.

Identifiants

pubmed: 36951434
doi: 10.1002/chem.202300780
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202300780

Informations de copyright

© 2023 Wiley-VCH GmbH.

Auteurs

Vinzenz Thönnißen (V)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Iuliana L Atodiresei (IL)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Frederic W Patureau (FW)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Classifications MeSH