Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review

Phenanthrenes and their aza-analogues have important applications in materials science and in medicine. Aim of this review is to collect recent reports describing their synthesis, which make use of radical cyclizations promoted by a visible light-triggered photocatalytic process.

Bibliographic Details
Main Authors:	Alessandra Del Tito, Havall Othman Abdulla, Davide Ravelli, Stefano Protti, Maurizio Fagnoni
Format:	Article
Language:	English
Published:	Beilstein-Institut 2020-06-01
Series:	Beilstein Journal of Organic Chemistry
Subjects:	phenanthrenes phenanthridines photocatalysis radicals visible light
Online Access:	https://doi.org/10.3762/bjoc.16.123

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spelling	doaj-5610ecf7a12145aa96089ff8c2572c9a2021-04-02T15:43:16ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972020-06-011611476148810.3762/bjoc.16.1231860-5397-16-123Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A reviewAlessandra Del Tito0Havall Othman Abdulla1Davide Ravelli2Stefano Protti3Maurizio Fagnoni4Photogreen Lab, Department of Chemistry, University of Pavia, Viale Taramelli 12, 27100 Pavia, ItalyPhotogreen Lab, Department of Chemistry, University of Pavia, Viale Taramelli 12, 27100 Pavia, ItalyPhotogreen Lab, Department of Chemistry, University of Pavia, Viale Taramelli 12, 27100 Pavia, ItalyPhotogreen Lab, Department of Chemistry, University of Pavia, Viale Taramelli 12, 27100 Pavia, ItalyPhotogreen Lab, Department of Chemistry, University of Pavia, Viale Taramelli 12, 27100 Pavia, ItalyPhenanthrenes and their aza-analogues have important applications in materials science and in medicine. Aim of this review is to collect recent reports describing their synthesis, which make use of radical cyclizations promoted by a visible light-triggered photocatalytic process.https://doi.org/10.3762/bjoc.16.123phenanthrenesphenanthridinesphotocatalysisradicalsvisible light
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Alessandra Del Tito Havall Othman Abdulla Davide Ravelli Stefano Protti Maurizio Fagnoni
spellingShingle	Alessandra Del Tito Havall Othman Abdulla Davide Ravelli Stefano Protti Maurizio Fagnoni Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review Beilstein Journal of Organic Chemistry phenanthrenes phenanthridines photocatalysis radicals visible light
author_facet	Alessandra Del Tito Havall Othman Abdulla Davide Ravelli Stefano Protti Maurizio Fagnoni
author_sort	Alessandra Del Tito
title	Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review
title_short	Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review
title_full	Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review
title_fullStr	Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review
title_full_unstemmed	Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review
title_sort	photocatalyzed syntheses of phenanthrenes and their aza-analogues. a review
publisher	Beilstein-Institut
series	Beilstein Journal of Organic Chemistry
issn	1860-5397
publishDate	2020-06-01
description	Phenanthrenes and their aza-analogues have important applications in materials science and in medicine. Aim of this review is to collect recent reports describing their synthesis, which make use of radical cyclizations promoted by a visible light-triggered photocatalytic process.
topic	phenanthrenes phenanthridines photocatalysis radicals visible light
url	https://doi.org/10.3762/bjoc.16.123
work_keys_str_mv	AT alessandradeltito photocatalyzedsynthesesofphenanthrenesandtheirazaanaloguesareview AT havallothmanabdulla photocatalyzedsynthesesofphenanthrenesandtheirazaanaloguesareview AT davideravelli photocatalyzedsynthesesofphenanthrenesandtheirazaanaloguesareview AT stefanoprotti photocatalyzedsynthesesofphenanthrenesandtheirazaanaloguesareview AT mauriziofagnoni photocatalyzedsynthesesofphenanthrenesandtheirazaanaloguesareview
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Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review

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