Hydroacenes made easy by gold(I) catalysis
Dorel, R.D.; McGonigal, P.R.; Echavarren, A.M.
Dr Paul Mcgonigal firstname.lastname@example.org
A novel strategy for the synthesis of partially saturated acene derivatives has been developed based on a AuI-catalyzed cyclization of 1,7-enynes. This method provides straightforward access to stable polycyclic products featuring the backbone of the acene series, up to nonacene.
Dorel, R., McGonigal, P., & Echavarren, A. (2016). Hydroacenes made easy by gold(I) catalysis. Angewandte Chemie International Edition, 55(37), 11120-11123. https://doi.org/10.1002/anie.201604952
|Journal Article Type||Article|
|Acceptance Date||Jun 14, 2016|
|Online Publication Date||Jul 6, 2016|
|Publication Date||Sep 5, 2016|
|Deposit Date||Jul 7, 2016|
|Publicly Available Date||Jul 6, 2017|
|Journal||Angewandte Chemie International Edition|
|Peer Reviewed||Peer Reviewed|
Accepted Journal Article
This is the peer reviewed version of the following article: Dorel, R., McGonigal, P. R. and Echavarren, A. M. (2016), Hydroacenes Made Easy by Gold(I). Angewandte Chemie International Edition, 55(37): 1120-1123, which has been published in final form at http://dx.doi.org/10.1002/anie.201604952. This article may be used for non-commercial purposes in accordance With Wiley-VCH Terms and Conditions for self-archiving.
You might also like
Control of Dynamic sp3-C Stereochemistry
Rupturing aromaticity by periphery overcrowding
Supramolecular Repair of Hydration Lubrication Surfaces