Enantioselective construction of the tricyclic core of curcusones A-D


Journal

Chemical science
ISSN: 2041-6520
Titre abrégé: Chem Sci
Pays: England
ID NLM: 101545951

Informations de publication

Date de publication:
07 Dec 2019
Historique:
received: 16 08 2019
accepted: 30 09 2019
entrez: 15 2 2020
pubmed: 15 2 2020
medline: 15 2 2020
Statut: epublish

Résumé

Herein we report our recent progress toward the enantioselective total synthesis of the diterpenoid natural products curcusones A-D by means of complementary Stetter annulation or ring-closing metathesis (RCM) disconnections. Using the latter approach, we have achieved the concise construction of the

Identifiants

pubmed: 32055379
doi: 10.1039/c9sc04127c
pii: c9sc04127c
pmc: PMC6988747
doi:

Types de publication

Journal Article

Langues

eng

Pagination

10562-10565

Informations de copyright

This journal is © The Royal Society of Chemistry 2019.

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Auteurs

Austin C Wright (AC)

Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering , Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , CA 91125 , USA . Email: stoltz@caltech.edu.

Brian M Stoltz (BM)

Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering , Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , CA 91125 , USA . Email: stoltz@caltech.edu.

Classifications MeSH