Selective synthesis of mono- and bis-butenolide α-aminomethyl adducts-Reference-Cited by-同舟云学术

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Selective synthesis of mono- and bis-butenolide α-aminomethyl adducts

Published:2017 Issue:15 Volume:15 Page:3298-3303
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Talbi Arbia¹²³⁴⁵,Arfaoui Aïcha¹²³⁴⁵,Bsaibess Talia⁶⁷⁸⁹,Lotfi Efrit Mohamed¹²³⁴⁵,Gaucher Anne⁶⁷⁸⁹,Prim Damien⁶⁷⁸⁹^ORCID,M′Rabet Hédi¹²³⁴⁵

Affiliation:

1. Université de Tunis El Manar

2. Faculté des Sciences de Tunis

3. Laboratoire de Synthèse Organique Sélective et Hétérocyclique-Evaluation de l'Activité Biologique

4. 2092 Tunis

5. Tunisia

6. Université de Versailles-Saint-Quentin

7. Institut Lavoisier de Versailles-UMR CNRS 8180

8. 78035 Versailles Cedex

9. France

Abstract

The preparation of mono- and bis-butenolide α-adducts is described using α-bromomethylene-γ-butenolide and primary as well as secondary amines.

Funder

Centre National de la Recherche Scientifique

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00206H

Reference60 articles.

1. Ancepsenolide: A novel bisbutenolide of marine origin

2. Ircinin-1 and -2, linear sesterterpenes from the marine sponge Ircinia oros

3. Fasciculatin, a novel sesterterpene from the sponge Ircinia fasciculata

4. Variabilin, an antibiotic from the sponge, ircinia variabilis

5. The structure of some antibiotics from the sponge

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