| Keyword search (4,163 papers available) | ![]() |
"Ottenwaelder X" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | Overlap and Covalency in a κN-Arylnitrosyl Cu(II) Metalloradical Formed by Hydroxylamine Oxidative Binding | MacKay A; Zsombor-Pindera J; Effaty F; Sheibany N; Gennarini F; Habibian M; Chen F; Askari MS; Brytskyi M; Kroeker S; Kennepohl P; Ottenwaelder X; | 41524899 CHEMBIOCHEM |
| 2 | Mechanochemistry for Metal-Organic Frameworks and Covalent-Organic Frameworks (MOFs, COFs): Methods, Materials, and Mechanisms | Marrett JM; Effaty F; Ottenwaelder X; Frišcic T; | 40708349 CHEMBIOCHEM |
| 3 | Mechanochemical Synthesis of Boroxine-linked Covalent Organic Frameworks | Hamzehpoor E; Effaty F; Borchers TH; Stein RS; Wahrhaftig-Lewis A; Ottenwaelder X; Frišcic T; Perepichka DF; | 38970305 CHEMBIOCHEM |
| 4 | Cooperative Sensitization Upconversion in Solution Dispersions of Co-Crystal Assemblies of Mononuclear Yb3+ and Eu3+ Complexes | Sun G; Xie Y; Wang Y; Mandl GA; Maurizio SL; Zhang H; Ottenwaelder X; Capobianco JA; Sun L; | 37040148 CNSR |
| 5 | Resonant acoustic mixing (RAM) for efficient mechanoredox catalysis without grinding or impact media | Effaty F; Gonnet L; Koenig SG; Nagapudi K; Ottenwaelder X; Frišcic T; | 36546478 CHEMBIOCHEM |
| 6 | Intramolecular H-bond stabilization of a primary hydroxylamine in salen-type metal complexes | Singh H; MacKay A; Sheibany N; Chen F; Mosser M; Rouet PÉ; Rousseau F; Askari MS; Ottenwaelder X; | 34545379 CHEMBIOCHEM |
| 7 | Programmed Synthesis of Tetra-Aryl Thiophenes with Stepwise, Ester-Controlled Regioselectivity | Messina C; Ottenwaelder X; Forgione P; | 34506149 CHEMBIOCHEM |
| 8 | Five Nitrogen Oxidation States from Nitro to Amine: Stabilization and Reactivity of a Metastable Arylhydroxylamine Complex. | Zsombor-Pindera J; Effaty F; Escomel L; Patrick B; Kennepohl P; Ottenwaelder X; | 33124796 CHEMBIOCHEM |
| 9 | Tuning Inner-Sphere Electron Transfer in a Series of Copper/Nitrosoarene Adducts. | Askari MS, Effaty F, Gennarini F, Orio M, Le Poul N, Ottenwaelder X | 32073833 CHEMBIOCHEM |
| 10 | A bio-inspired synthesis of oxindoles by catalytic aerobic dual C-H functionalization of phenols. | Huang Z, Askari MS, Esguerra KVN, Dai TY, Kwon O, Ottenwaelder X, Lumb JP | 29861988 CHEMISTRY |
| 11 | Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions. | Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A | 27231755 CHEMBIOCHEM |
| 12 | Supramolecular control of monooxygenase reactivity in a copper(ii) cryptate. | Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X | 27328176 CHEMBIOCHEM |
| Title: | Programmed Synthesis of Tetra-Aryl Thiophenes with Stepwise, Ester-Controlled Regioselectivity | ||||
| Authors: | Messina C, Ottenwaelder X, Forgione P | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/34506149/ | ||||
| DOI: | 10.1021/acs.orglett.1c02447 | ||||
| Publication: | Organic letters | ||||
| Keywords: | |||||
| PMID: | 34506149 | Category: | Date Added: | 2021-09-11 | |
| Dept Affiliation: |
CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Concordia University, Montreal, Quebec H4B 1R6, Canada. |
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Description: |
Herein, we report a modular synthetic route to access tetra-arylated thiophene compounds with four different substituents with programmed chemical control provided by an ester activating/directing group. This method enables the functionalization of individual positions of thiophene sequentially via regioselective halogenations and cross-coupling reactions. The reaction sequence described provides tetra-arylated thiophenes in higher yields than previous routes and employs practical reaction protocols, simple catalytic systems, and short reaction times. |



