Enantioselective syntheses of indanes: from organocatalysis to C–H functionalization-Reference-Cited by-同舟云学术

Enantioselective syntheses of indanes: from organocatalysis to C–H functionalization

Published:2016 Issue:5 Volume:45 Page:1368-1386
ISSN:0306-0012
Container-title:Chemical Society Reviews
language:en
Short-container-title:Chem. Soc. Rev.

Author:

Borie Cyril¹²³⁴⁵,Ackermann Lutz⁶⁷⁸⁹,Nechab Malek¹²³⁴⁵

Affiliation:

1. Aix Marseille Université CNRS

2. ICR

3. UMR 7273

4. 13013 Marseille

5. France

6. Institut fuer Organische und Biomolekulare Chemie

7. Georg-August-Universitaet Goettingen

8. 37077 Goettingen

9. Germany

Abstract

The indanyl core is ubiquitous in a large variety of drugs and natural products. Remarkable recent progress has been accomplished in the step-economical assembly of functionalization of chiral indanes by means of enantioselective catalysis, with major progress being achieved in organocatalysis and C–H activation chemistry.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CS/C5CS00622H

Reference158 articles.

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3. Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Asymmetric Stetter Reaction

4. A New Copper Acetate-Bis(oxazoline)-Catalyzed, Enantioselective Henry Reaction

5. An organic thiyl radical catalyst for enantioselective cyclization

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