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Analysis of institutional authors

García Suero, MarcosAuthor

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October 7, 2019
Publications
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Review

New Alkene Cyclopropanation Reactions Enabled by Photoredox Catalysis via Radical Carbenoids

Publicated to: Synthesis-Stuttgart. 51 (14): 2821-2828 - 2019-07-16 51(14), DOI: 10.1055/s-0037-1611872

Authors:

Herraiz, AG; Suero, MG
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Affiliations

Barcelona Inst Sci & Technol, Inst Chem Res Catalonia ICIQ, Paisos Catalans 16, Tarragona 43007, Spain - Author
Barcelona Institute of Science and Technology (BIST) - Author
Univ Rovira & Virgili, Dept Quim Analit & Quim Organ, C Marcelli Domingo 1, E-43007 Tarragona, Spain - Author
Universitat Rovira i Virgili - Author
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Abstract

© Georg Thieme Verlag Stuttgart New York. We describe the recent emergence of a new approach for the synthesis of cyclopropane rings by means of photoredox catalysis. This methodology relies on the photocatalytic generation of radical carbenoids or carbenoid-like radicals as cyclopropanating species, and is characterized by excellent functional group tolerance, chemoselectivity and the ability to form cyclopropanes with excellent control from E / Z alkene mixtures. The mild reaction conditions and employment of user-friendly reagents are highly attractive features that may lead to this approach being used in academic and industrial laboratories. 1 Introduction 2 Photoredox-Catalyzed Alkene Cyclopropanations with Radical Carbenoids 3 Conclusions and Outlook.
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Keywords

Alkyl-halidesCarbenoidsCationCyclizationCyclopropanationCyclopropanesDerivativesIodidesPhotochemistryPhotolysisPhotoredox catalysisRadicals

Quality index

Bibliometric impact. Analysis of the contribution and dissemination channel

The work has been published in the journal SYNTHESIS-STUTTGART due to its progression and the good impact it has achieved in recent years, according to the agency Scopus (SJR), it has become a reference in its field. In the year of publication of the work, 2019, it was in position , thus managing to position itself as a Q1 (Primer Cuartil), in the category Organic Chemistry.

From a relative perspective, and based on the normalized impact indicator calculated from World Citations provided by WoS (ESI, Clarivate), it yields a value for the citation normalization relative to the expected citation rate of: 1.5. This indicates that, compared to works in the same discipline and in the same year of publication, it ranks as a work cited above average. (source consulted: ESI Nov 13, 2025)

Specifically, and according to different indexing agencies, this work has accumulated citations as of 2026-03-15, the following number of citations:

  • WoS: 28
  • Scopus: 11
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Impact and social visibility

From the perspective of influence or social adoption, and based on metrics associated with mentions and interactions provided by agencies specializing in calculating the so-called "Alternative or Social Metrics," we can highlight as of 2026-03-15:

  • The use, from an academic perspective evidenced by the Altmetric agency indicator referring to aggregations made by the personal bibliographic manager Mendeley, gives us a total of: 30.
  • The use of this contribution in bookmarks, code forks, additions to favorite lists for recurrent reading, as well as general views, indicates that someone is using the publication as a basis for their current work. This may be a notable indicator of future more formal and academic citations. This claim is supported by the result of the "Capture" indicator, which yields a total of: 30 (PlumX).

With a more dissemination-oriented intent and targeting more general audiences, we can observe other more global scores such as:

  • The Total Score from Altmetric: 13.
  • The number of mentions on the social network X (formerly Twitter): 23 (Altmetric).

It is essential to present evidence supporting full alignment with institutional principles and guidelines on Open Science and the Conservation and Dissemination of Intellectual Heritage. A clear example of this is:

  • The work has been submitted to a journal whose editorial policy allows open Open Access publication.
  • Assignment of a Handle/URN as an identifier within the deposit in the Institutional Repository: http://hdl.handle.net/2072/359749
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Leadership analysis of institutional authors

There is a significant leadership presence as some of the institution’s authors appear as the first or last signer, detailed as follows: First Author (Herraiz A) and Last Author (Suero M).

the author responsible for correspondence tasks has been Suero M.

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