Formal Cycloadditions Driven by the Homolytic Opening of Strained, Saturated Ring Systems
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Formal Cycloadditions Driven by the Homolytic Opening of Strained, Saturated Ring Systems ; day:30 ; month:11 ; year:2022 ; extent:1
Angewandte Chemie ; (30.11.2022) (gesamt 1)
- Creator
- DOI
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10.1002/ange.202213003
- URN
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urn:nbn:de:101:1-2022120114184731067728
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:31 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Harmata, Alexander S.
- Roldan, B. J.
- Stephenson, Corey R. J.
Other Objects (12)
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Gold-Catalyzed Formal Cycloadditions of Alkynes for Azaheterocycle Syntheses
Continuous Flow Bioconjugations of NIR‐AZA Fluorophores via Strained Alkyne Cycloadditions with Intra‐Chip Fluorogenic Monitoring **
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
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1,2‐Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles
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Cycloadditions to 1,1-Dicyclopropylethylene
Formal Cycloadditions Driven by the Homolytic Opening of Strained, Saturated Ring Systems
Ring-opening metathesis of some strained bicyclic systems; stereocontrolled access to diolefinated saturated heterocycles with multiple stereogenic centers
Gold-catalyzed formal cycloadditions of alkynes for azaheterocycle syntheses
Gold-Catalyzed Formal Cycloadditions of Alkynes for Azaheterocycle Syntheses
Continuous Flow Bioconjugations of NIR‐AZA Fluorophores via Strained Alkyne Cycloadditions with Intra‐Chip Fluorogenic Monitoring **
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
Chiral auxiliaries in cycloadditions
Diastereoselective [4+4] Cycloadditions
1,2‐Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles
Dearomative Cycloadditions Catalyzed by Palladium
Cycloadditions to 1,1-Dicyclopropylethylene
Formal Cycloadditions Driven by the Homolytic Opening of Strained, Saturated Ring Systems
Ring-opening metathesis of some strained bicyclic systems; stereocontrolled access to diolefinated saturated heterocycles with multiple stereogenic centers
Gold-catalyzed formal cycloadditions of alkynes for azaheterocycle syntheses
Gold-Catalyzed Formal Cycloadditions of Alkynes for Azaheterocycle Syntheses
Continuous Flow Bioconjugations of NIR‐AZA Fluorophores via Strained Alkyne Cycloadditions with Intra‐Chip Fluorogenic Monitoring **
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
Synthesis of 2‐Azanorbornanes via Strain‐Release Formal Cycloadditions Initiated by Energy Transfer
Chiral auxiliaries in cycloadditions
Diastereoselective [4+4] Cycloadditions
1,2‐Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles
Dearomative Cycloadditions Catalyzed by Palladium