Auto tandem triple cascade organocatalysis: access to bis-lactone and butenolide derivatives-Reference-Cited by-同舟云学术

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Auto tandem triple cascade organocatalysis: access to bis-lactone and butenolide derivatives

Published:2024 Issue:69 Volume:60 Page:9278-9281
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wittmann Stéphane¹,Deschamps Elodie¹,Bournaud Chloée¹,Guillot Regis¹^ORCID,Brière Jean-François²^ORCID,Vo-Thanh Giang¹^ORCID,Toffano Martial¹^ORCID

Affiliation:

1. Institut de Chimie Moléculaire et des Matériaux d’Orsay, CNRS-UMR-8182, Université Paris-Saclay, Bât. H. Moissan. 19 avenue des sciences, 91400 Orsay, France

2. Normandie Univ, UNIROUEN, INSA Rouen, CNRS, COBRA, 76000 Rouen, France

Abstract

A triple cascade auto tandem process catalyzed by the same catalytic specie leads to bis-lastone and butenolides in a stereoselective manner.

Funder

Centre National de la Recherche Scientifique

Université Paris-Saclay

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC03029J

Reference27 articles.

1. Sesquiterpenes and Alkaloids from Lindera chunii and Their Inhibitory Activities against HIV-1 Integrase.

2. New abietane diterpenoids from the roots of Salvia przewalskii

3. First total synthesis of (−)-salprzelactone

4. Bielschowskysin, a Gorgonian-Derived Biologically Active Diterpene with an Unprecedented Carbon Skeleton

5. Regioselectivity of dimerisation of butenolides via captodative stabilised radicaloid intermediates

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