Perylene Synthesis by the Parallel Cycloaromatization of Adjacent Enediynes

As part of an investigation into new synthetic routes to poly(peri-naphthalene), the synthesis and cycloaromatization of tetraethynylbiphenyls is described. The temperature-dependent cyclization of biphenyls containing unsubstituted alkynes provides the desired perylene in good yield.

Tags
Data and Resources
To access the resources you must log in

This item has no data

Identity

Description: The Identity category includes attributes that support the identification of the resource.

Field Value
PID https://www.doi.org/10.1021/ol005615f
PID https://www.doi.org/10.1021/ol005615f.s001
URL http://dx.doi.org/10.1021/ol005615f
URL https://figshare.com/articles/journal_contribution/Perylene_Synthesis_by_the_Parallel_Cycloaromatization_of_Adjacent_Enediynes/3735738
URL https://academic.microsoft.com/#/detail/2949600893
URL https://pubs.acs.org/doi/pdf/10.1021/ol005615f
URL https://pubs.acs.org/doi/10.1021/ol005615f
URL https://www.ncbi.nlm.nih.gov/pubmed/10768197
Access Modality

Description: The Access Modality category includes attributes that report the modality of exploitation of the resource.

Field Value
Access Right Open Access
Attribution

Description: Authorships and contributors

Field Value
Author Chow, Siew-Yin
Author Palmer, Grant J.
Author Bowles, Daniel M.
Author Anthony, John E.
Publishing

Description: Attributes about the publishing venue (e.g. journal) and deposit location (e.g. repository)

Field Value
Collected From figshare; Crossref; Microsoft Academic Graph
Hosted By Organic Letters; figshare
Journal Organic Letters, 2, null
Publication Date 2016-08-20
Publisher American Chemical Society (ACS)
Additional Info
Field Value
Language Undetermined
Resource Type Other literature type; Article
system:type publication
Management Info
Field Value
Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::1cd3979de2346295b84315e97fcc6483
Author jsonws_user
Last Updated 27 December 2020, 03:04 (CET)
Created 27 December 2020, 03:04 (CET)