David Cruz Cruz

Dr. David Cruz Cruz

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 April 2021 in Chemistry – A European Journal
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Journal Article
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AFAlberto Feliciano
Alberto Feliciano
JVJuan L. Vázquez
Juan L. Vázquez
LBLuis J. Benítez‐Puebla
Luis J. Benítez‐Puebla
IVIván Velazco‐Cabral
Iván Velazco‐Cabral
DCDavid Cruz Cruz
David Cruz Cruz
MVMiguel Vazquez
Miguel Vazquez

20 March 2019 in Chemical Science
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Journal Article
Open access
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AGAndrea Guerrero-Corella
Andrea Guerrero-Corella
JAJuan Asenjo-Pascual
Juan Asenjo-Pascual
Tushar Janardan PawarTushar Janardan Pawar
Tushar Janardan Pawar
SDSergio Diaz-Tendero
Sergio Diaz-Tendero
Ana Martin-SomerAna Martin-Somer
Ana Martin-Somer
José AlemánJosé Alemán
José Alemán
In this work we have found that a BODIPY can be used as an electron withdrawing group for the activation of double bonds in asymmetric catalysis. The synthesis of cyclohexyl derivatives containing a BODIPY unit can easily be achieved via trienamine catalysis. This allows a new different asymmetric synthesis of BODIPY derivatives and opens the door to future transformation of this useful fluorophore. In addition, the Quantum Chemistry calculations and mechanistic studies provide insights into the role of BODIPY as an EWG.

23 April 2014 in Chemical Communications
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CVClarisa Villegas-Gómez
Clarisa Villegas-Gómez
DCDavid Cruz Cruz
David Cruz Cruz
RMRasmus Mose
Rasmus Mose
KJKarl Anker Jørgensen
Karl Anker Jørgensen
The organocatalytic enantioselective synthesis of highly functionalized hydroisoquinolines by trienamine-mediated [4+2]-cycloaddition/nucleophilic ring-closing reaction cascade sequence of cyanoacrylamides with 2,4-dienals is presented.

3 May 2012 in Chemical Communications
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DCDavid Cruz Cruz
David Cruz Cruz
PSPedro A. Sánchez-Murcia
Pedro A. Sánchez-Murcia
KJKarl Anker Jørgensen
Karl Anker Jørgensen
A formal asymmetric organocatalytic aminohydroxylation reaction of enones has been achieved via an aziridination–double SN2 sequence. As a part of the reaction design, the generated amino alcohol products are isolated as the corresponding oxazolidinones in good yields and excellent stereoselectivities.

5 June 2020 in European Journal of Organic Chemistry
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Journal Article
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Tushar Janardan PawarTushar Janardan Pawar
Tushar Janardan Pawar
SMSuhas Balasaheb Mitkari
Suhas Balasaheb Mitkari
EPEduardo Peña-Cabrera
Eduardo Peña-Cabrera
CVClarisa Villegas-Gómez
Clarisa Villegas-Gómez
DCDavid Cruz Cruz
David Cruz Cruz

9 November 2020 in Chemistry – A European Journal
Verified
Journal Article
Closed access
PDF file
SMSuhas Balasaheb Mitkari
Suhas Balasaheb Mitkari
AMAlberto Medina‐Ortíz
Alberto Medina‐Ortíz
JOJosé Luis Olivares-Romero
José Luis Olivares-Romero
MVMiguel Vazquez
Miguel Vazquez
EPEduardo Peña-Cabrera
Eduardo Peña-Cabrera
DCDavid Cruz Cruz
David Cruz Cruz