Journal
CHEMICAL REVIEWS
Volume 116, Issue 17, Pages 9748-9815Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.5b00723
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Funding
- European Research Council under the European Union's Horizon research and innovation program [665951 - ELICOS]
- Deutsche Forschungsgemeinschaft (Reinhart Koselleck program) [SPP 1179, Ba1372/11, Ba1372/6]
- Alexander von Humboldt foundation
- TU Munchen
- Fonds der Chemischen Industrie
- Elitenetzwerk Bayern
- Roche Postdoc Fellowship (RPF) program
- Sanofi-Aventis
- Astra Zeneca Research Award in Organic Chemistry
- Novartis Young European Investigator Award
- Degussa Prize for Chirality in Chemistry
- Graduiertenkolleg 1626 Chemische Photokatalyse
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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 televant, regio-, and stereoselcctive 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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