Keyword search (4,164 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:Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions.
Authors:Hébert MPetiot PBenoit EDansereau JAhmad TLe Roch AOttenwaelder XGagnon A
Link:https://www.ncbi.nlm.nih.gov/pubmed/27231755?dopt=Abstract
Publication:
Keywords:
PMID:27231755 Category:J Org Chem Date Added:2019-05-31
Dept Affiliation: CHEMBIOCHEM
1 Université du Québec à Montréal , Département de Chimie, C.P. 8888, Succursale Centre-Ville, Montréal, Québec, Canada , H3C 3P8.
2 Concordia University , Department of Chemistry and Biochemistry, 7141 Sherbrooke Street West, Montréal, Québec, Canada , H4B 1R6.

Description:

Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions.

J Org Chem. 2016 07 01;81(13):5401-16

Authors: Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A

Abstract

Organobismuthines are an attractive class of organometallic reagents that can be accessed from inexpensive and nontoxic bismuth salts. Triarylbismuthines are particularly interesting due to their air and moisture stability and high functional group tolerance. We report herein a detailed study on the preparation of highly functionalized triarylbismuth reagents by triple functional group manipulation and their use in palladium- and copper-catalyzed C-, N-, and O-arylation reactions.

PMID: 27231755 [PubMed]





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