A sequential cyclization/π-extension strategy for modular construction of nanographenes enabled by stannole cycloadditions-Reference-Cited by-同舟云学术

A sequential cyclization/π-extension strategy for modular construction of nanographenes enabled by stannole cycloadditions

Published:2022 Issue:19 Volume:13 Page:5568-5573
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Bergman Harrison M.¹^ORCID,Beattie D. Dawson¹,Kiel Gavin R.¹^ORCID,Handford Rex C.¹,Liu Yi²^ORCID,Tilley T. Don¹^ORCID

Affiliation:

1. Department of Chemistry, University of California, Berkeley, California 94720, USA

2. Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA

Abstract

Stannoles are introduced as a new, spontaneously aromatizing diene for [4 + 2] cycloadditions that can be easily introduced into diverse conjugated systems, facilitating the efficient synthesis of complex PAHs and their π-extension.

Funder

Division of Chemistry

U.S. Department of Energy

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/SC/D2SC00397J

Reference33 articles.

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