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Royal Society of Chemistry, Chemical Science, 9(6), p. 5164-5171, 2015

DOI: 10.1039/c5sc01909e

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

Journal article published in 2015 by J. Pedroni, T. Saget, P. A. Donets ORCID, N. Cramer
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

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. This journal is