Jordi Torró
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jordi Torró has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Amparo Sanz-Marco
Departament de Química Orgànica, Facultat de Química, Universitat de València, C. Dr. Moliner 50, 46100 Burjassot, Spain
1 shared publication - Carlos Vila
Departament de Química Orgànica, Facultat de Química, Universitat de València, C. Dr. Moliner 50, 46100 Burjassot, Spain
1 shared publication - Gonzalo Blay
Departament de Química Orgànica, Facultat de Química, Universitat de València, C. Dr. Moliner 50, 46100 Burjassot, Spain
1 shared publication - Ricardo Torán
Departament de Química Orgànica, Facultat de Química, Universitat de València, C. Dr. Moliner 50, 46100 Burjassot, Spain
1 shared publication
Latest Publications
- Open Access
- 28 April 2025
- Published by Wiley in ChemCatChem
- Vol. 17 (12)
Organocatalytic Enantioselective Conjugate Addition of Isoxazol‐5(4 H )‐Ones to Aurone‐Derived Azadienes
An efficient enantioselective organocatalytic conjugate addition of isoxazol‐5(4 H )‐ones to aurone‐derived azadienes under mild conditions has been developed. This methodology provides access to a wide range of chiral compounds featuring both benzofuran and isoxazole scaffolds in their structures achieving high yields and stereo control. Furthermore, the resulting adducts can be readily transformed into chiral β‐benzofuran‐branched carbonyl compounds in high yields and enantioselectivity in one‐pot reaction through hydrolysis‐decarboxylation of the isoxazole ring.
- 28 April 2025
- Published by Wiley in ChemCatChem
- Vol. 17 (12)
Open AccessOrganocatalytic Enantioselective Conjugate Addition of Isoxazol‐5(4 H )‐Ones to Aurone‐Derived Azadienes
An efficient enantioselective organocatalytic conjugate addition of isoxazol‐5(4 H )‐ones to aurone‐derived azadienes under mild conditions has been developed. This methodology provides access to a wide range of chiral compounds featuring both benzofuran and isoxazole scaffolds in their structures achieving high yields and stereo control. Furthermore, the resulting adducts can be readily transformed into chiral β‐benzofuran‐branched carbonyl compounds in high yields and enantioselectivity in one‐pot reaction through hydrolysis‐decarboxylation of the isoxazole ring.