Organocatalytic Enantioselective Conjugate Addition of Isoxazol‐5(4H)‐Ones to Aurone‐Derived Azadienes.
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| Title: | Organocatalytic Enantioselective Conjugate Addition of Isoxazol‐5(4H)‐Ones to Aurone‐Derived Azadienes. |
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| Authors: | Torán, Ricardo1 (AUTHOR), Torró, Jordi1 (AUTHOR), Sanz‐Marco, Amparo1 (AUTHOR) amparo.sanz-marco@uv.es, Vila, Carlos1 (AUTHOR), Blay, Gonzalo1 (AUTHOR) gonzalo.blay@uv.es |
| Source: | ChemCatChem. 6/23/2025, Vol. 17 Issue 12, p1-5. 5p. |
| Subjects: | Organocatalysis, Conjugate addition reactions, Stereoselective reactions, Azaarenes, Benzofuran, Isoxazoles, Chiral drugs, Aurones |
| Abstract: | An efficient enantioselective organocatalytic conjugate addition of isoxazol‐5(4H)‐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. [ABSTRACT FROM AUTHOR] |
| Copyright of ChemCatChem is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
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| Header | DbId: egs DbLabel: Engineering Source An: 186461225 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Organocatalytic Enantioselective Conjugate Addition of Isoxazol‐5(4H)‐Ones to Aurone‐Derived Azadienes. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Torán%2C+Ricardo%22">Torán, Ricardo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Torró%2C+Jordi%22">Torró, Jordi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sanz‐Marco%2C+Amparo%22">Sanz‐Marco, Amparo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> amparo.sanz-marco@uv.es</i><br /><searchLink fieldCode="AR" term="%22Vila%2C+Carlos%22">Vila, Carlos</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Blay%2C+Gonzalo%22">Blay, Gonzalo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> gonzalo.blay@uv.es</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22ChemCatChem%22">ChemCatChem</searchLink>. 6/23/2025, Vol. 17 Issue 12, p1-5. 5p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Organocatalysis%22">Organocatalysis</searchLink><br /><searchLink fieldCode="DE" term="%22Conjugate+addition+reactions%22">Conjugate addition reactions</searchLink><br /><searchLink fieldCode="DE" term="%22Stereoselective+reactions%22">Stereoselective reactions</searchLink><br /><searchLink fieldCode="DE" term="%22Azaarenes%22">Azaarenes</searchLink><br /><searchLink fieldCode="DE" term="%22Benzofuran%22">Benzofuran</searchLink><br /><searchLink fieldCode="DE" term="%22Isoxazoles%22">Isoxazoles</searchLink><br /><searchLink fieldCode="DE" term="%22Chiral+drugs%22">Chiral drugs</searchLink><br /><searchLink fieldCode="DE" term="%22Aurones%22">Aurones</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: An efficient enantioselective organocatalytic conjugate addition of isoxazol‐5(4H)‐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. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of ChemCatChem is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=186461225 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/cctc.202500033 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Subjects: – SubjectFull: Organocatalysis Type: general – SubjectFull: Conjugate addition reactions Type: general – SubjectFull: Stereoselective reactions Type: general – SubjectFull: Azaarenes Type: general – SubjectFull: Benzofuran Type: general – SubjectFull: Isoxazoles Type: general – SubjectFull: Chiral drugs Type: general – SubjectFull: Aurones Type: general Titles: – TitleFull: Organocatalytic Enantioselective Conjugate Addition of Isoxazol‐5(4H)‐Ones to Aurone‐Derived Azadienes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Torán, Ricardo – PersonEntity: Name: NameFull: Torró, Jordi – PersonEntity: Name: NameFull: Sanz‐Marco, Amparo – PersonEntity: Name: NameFull: Vila, Carlos – PersonEntity: Name: NameFull: Blay, Gonzalo IsPartOfRelationships: – BibEntity: Dates: – D: 23 M: 06 Text: 6/23/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 18673880 Numbering: – Type: volume Value: 17 – Type: issue Value: 12 Titles: – TitleFull: ChemCatChem Type: main |
| ResultId | 1 |