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Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions

[Image: see text] The [2 + 2] photocycloaddition is undisputedly the most important and most frequently used photochemical reaction. In this review, it is attempted to cover all recent aspects of [2 + 2] photocycloaddition chemistry with an emphasis on synthetically relevant, regio-, and stereoselec...

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Autores principales: Poplata, Saner, Tröster, Andreas, Zou, You-Quan, Bach, Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025837/
https://www.ncbi.nlm.nih.gov/pubmed/27018601
http://dx.doi.org/10.1021/acs.chemrev.5b00723
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author Poplata, Saner
Tröster, Andreas
Zou, You-Quan
Bach, Thorsten
author_facet Poplata, Saner
Tröster, Andreas
Zou, You-Quan
Bach, Thorsten
author_sort Poplata, Saner
collection PubMed
description [Image: see text] The [2 + 2] photocycloaddition is undisputedly the most important and most frequently used photochemical reaction. In this review, it is attempted to cover all recent aspects of [2 + 2] photocycloaddition chemistry with an emphasis on synthetically relevant, regio-, and stereoselective reactions. The review aims to comprehensively discuss relevant work, which was done in the field in the last 20 years (i.e., from 1995 to 2015). Organization of the data follows a subdivision according to mechanism and substrate classes. Cu(I) and PET (photoinduced electron transfer) catalysis are treated separately in sections 2 and 4, whereas the vast majority of photocycloaddition reactions which occur by direct excitation or sensitization are divided within section 3 into individual subsections according to the photochemically excited olefin.
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spelling pubmed-50258372016-09-19 Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions Poplata, Saner Tröster, Andreas Zou, You-Quan Bach, Thorsten Chem Rev [Image: see text] The [2 + 2] photocycloaddition is undisputedly the most important and most frequently used photochemical reaction. In this review, it is attempted to cover all recent aspects of [2 + 2] photocycloaddition chemistry with an emphasis on synthetically relevant, regio-, and stereoselective reactions. The review aims to comprehensively discuss relevant work, which was done in the field in the last 20 years (i.e., from 1995 to 2015). Organization of the data follows a subdivision according to mechanism and substrate classes. Cu(I) and PET (photoinduced electron transfer) catalysis are treated separately in sections 2 and 4, whereas the vast majority of photocycloaddition reactions which occur by direct excitation or sensitization are divided within section 3 into individual subsections according to the photochemically excited olefin. American Chemical Society 2016-03-28 2016-09-14 /pmc/articles/PMC5025837/ /pubmed/27018601 http://dx.doi.org/10.1021/acs.chemrev.5b00723 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Poplata, Saner
Tröster, Andreas
Zou, You-Quan
Bach, Thorsten
Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions
title Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions
title_full Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions
title_fullStr Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions
title_full_unstemmed Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions
title_short Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions
title_sort recent advances in the synthesis of cyclobutanes by olefin [2 + 2] photocycloaddition reactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025837/
https://www.ncbi.nlm.nih.gov/pubmed/27018601
http://dx.doi.org/10.1021/acs.chemrev.5b00723
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