Synthesis of Medium-Sized Carbocycles via a Bidentate Lewis Acid-Catalyzed Inverse Electron-Demand Diels–Alder Reaction Followed by Photoinduced Ring-Opening
Author:
Affiliation:
1. Institute of Organic Chemistry, Justus Liebig University Giessen, Heinrich-Buff-Ring 17, 35392 Giessen, Germany
2. Center for Materials Research (LaMa), Justus Liebig University Giessen, Heinrich-Buff-Ring 16, 35392 Giessen, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c00249
Reference57 articles.
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4. Multiple Metal–Carbon Bonds for Catalytic Metathesis Reactions (Nobel Lecture)
5. Synthesis of chiral molybdenum ROMP initiators and all-cis highly tactic poly(2,3-(R)2norbornadiene) (R = CF3 or CO2Me)
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1. Bidentate Lewis Acid-Catalyzed Inverse Electron-Demand Diels–Alder Reaction of Phthalazines and Cyclooctynes;Synlett;2023-11-06
2. Six-membered ring systems: diazines and benzo derivatives;Progress in Heterocyclic Chemistry;2023
3. Mechanistic Studies on the Bidentate Lewis Acid Catalyzed Domino Inverse Electron‐Demand Diels‐Alder/Thiol Transfer Reaction;European Journal of Organic Chemistry;2022-12-27
4. Kinetically Controllable Construction of Nine-Membered Carbocycles via Pd-Catalyzed Decarboxylative Cycloaddition;Organic Letters;2022-03-28
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