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  4. Enantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system
 
research article

Enantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system

Pedroni, J.  
•
Saget, T.  
•
Donets, P. A.  
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2015
Chemical Science

Taddol-based phosphoramidite ligands enable enantioselective palladium(0)-catalyzed C-H arylation of cyclopropanes. The cyclized products are obtained in high yields and enantioselectivities. The reported method provides efficient access to a broad range of synthetically attractive cyclopropyl containing dihydroquinolones and dihydroisoquinolones as well as allows for an efficient enantioselective construction of the 7-membered ring of the cyclopropyl indolobenzazepine core of BMS-791325.

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Type
research article
DOI
10.1039/c5sc01909e
Web of Science ID

WOS:000359214100009

Author(s)
Pedroni, J.  
Saget, T.  
Donets, P. A.  
Cramer, N.  
Date Issued

2015

Publisher

Royal Soc Chemistry

Published in
Chemical Science
Volume

6

Issue

9

Start page

5164

End page

5171

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSA  
Available on Infoscience
September 28, 2015
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/119072
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