A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone-Reference-Cited by-同舟云学术

A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone

Published:2016 Issue:39 Volume:52 Page:6565-6568
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Ren Yajun¹²³⁴⁵,Presset Marc¹²³⁴⁵,Godemert Jeremy¹²³⁴⁵,Vanthuyne Nicolas¹²³⁴⁵,Naubron Jean-Valère¹³⁶⁵⁷,Giorgi Michel¹³⁶⁵⁷,Rodriguez Jean¹²³⁴⁵,Coquerel Yoann¹²³⁴⁵

Affiliation:

1. Aix Marseille Université

2. Centrale Marseille

3. CNRS

4. iSm2 UMR7313

5. F-13397 Marseille

6. Spectropole FR1739

7. France

Abstract

Switch it! The combination of aminocatalysis and N-heterocyclic carbene catalysis has been extended to a switchable dual catalytic system.

Funder

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C6CC01689H

Reference39 articles.

1. Quadrane Sesquiterpenes: Natural Sources, Biology, and Syntheses

2. Natural products: A continuing source of novel drug leads

3. Enantioselective Total Synthesis of Isishippuric Acid B via Intramolecular Michael Reaction

4. Determination of the Absolute Configurations of Natural Products via Density Functional Theory Calculations of Optical Rotation, Electronic Circular Dichroism, and Vibrational Circular Dichroism: The Cytotoxic Sesquiterpene Natural Products Quadrone, Suberosenone, Suberosanone, and Suberosenol A Acetate

5. First enantioselective total synthesis and configurational assignments of suberosenone and suberosanone as potential antitumor agents

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