Directed ortho-metalation–nucleophilic acyl substitution strategies in deep eutectic solvents: the organolithium base dictates the chemoselectivity-Reference-Cited by-同舟云学术

Directed ortho-metalation–nucleophilic acyl substitution strategies in deep eutectic solvents: the organolithium base dictates the chemoselectivity

Published:2019 Issue:54 Volume:55 Page:7741-7744
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Ghinato Simone¹²³⁴^ORCID,Dilauro Giuseppe⁵⁶⁷⁸⁴^ORCID,Perna Filippo Maria⁵⁶⁷⁸⁴^ORCID,Capriati Vito⁵⁶⁷⁸⁴^ORCID,Blangetti Marco¹²³⁴^ORCID,Prandi Cristina¹²³⁴^ORCID

Affiliation:

1. Dipartimento di Chimica

2. Università di Torino

3. I-10125 Torino

4. Italy

5. Dipartimento di Farmacia-Scienze del Farmaco

6. Università di Bari “A. Moro”

7. Consorzio C.I.N.M.P.I.S.

8. I-70125 Bari

Abstract

Organolithium-mediated chemoselectivity in deep eutectic solvents: basicity vs. nucleophilicity.

Funder

Ministero dell'Istruzione, dell'Università e della Ricerca

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/2019/CC/C9CC03927A

Reference45 articles.

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5. Concise Total Syntheses of (+)-Haplocidine and (+)-Haplocine via Late-Stage Oxidation of (+)-Fendleridine Derivatives

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