Directed Ortho and Remote Metalation of Naphthalene 1,8-Diamide: Complementing SEAr Reactivity for the Synthesis of Substituted Naphthalenes-Reference-Cited by-同舟云学术

Directed Ortho and Remote Metalation of Naphthalene 1,8-Diamide: Complementing SEAr Reactivity for the Synthesis of Substituted Naphthalenes

Published:2021-03-05 Issue:6 Volume:23 Page:1966-1973
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Jones Christopher C. V.¹^ORCID,Patel Jignesh J.¹,Jansen-van Vuuren Ross D.¹^ORCID,Ross Gregory M.²,Keller Bernd O.³,Sauriol Francoise¹,Schatte Gabriele¹,Johnson Erin R.⁴^ORCID,Snieckus Victor¹^ORCID

Affiliation:

1. Department of Chemistry, Queen’s University, Kingston, ON K7L 3N6, Canada

2. Northern Ontario School of Medicine, Laurentian University, Sudbury, ON P3E 2C6, Canada

3. Numinus Bioscience, Nanaimo, BC V9R 6Z8, Canada

4. Department of Chemistry, Dalhousie University, Halifax, NS B3H 4R2, Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c00521

Reference91 articles.

1. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products

2. Method for the Rapid Synthesis of Highly Functionalized 2-Hydroxy-1-naphthoates. Syntheses of the Naphthoic Acid Components of Neocarzinostatin Chromophore and N1999A2

3. Naphthalene, a versatile platform in medicinal chemistry: Sky-high perspective

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