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Tuning Inner-Sphere Electron Transfer in a Series of Copper/Nitrosoarene Adducts.

Author(s): Askari MS, Effaty F, Gennarini F, Orio M, Le Poul N, Ottenwaelder X

Inorg Chem. 2020 Feb 19;: Authors: Askari MS, Effaty F, Gennarini F, Orio M, Le Poul N, Ottenwaelder X

Article GUID: 32073833
A bio-inspired synthesis of oxindoles by catalytic aerobic dual C-H functionalization of phenols.

Author(s): Huang Z, Askari MS, Esguerra KVN, Dai TY, Kwon O, Ottenwaelder X, Lumb JP

Chem Sci. 2016 Jan 01;7(1):358-369 Authors: Huang Z, Askari MS, Esguerra KVN, Dai TY, Kwon O, Ottenwaelder X, Lumb JP

Article GUID: 29861988
Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions.

Author(s): Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A

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

Article GUID: 27231755
Supramolecular control of monooxygenase reactivity in a copper(ii) cryptate.

Author(s): Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X

Dalton Trans. 2016 Jul 05;45(27):11109-19 Authors: Chaloner L, Khomutovskaya A, Thomas F, Ottenwaelder X

Article GUID: 27328176
Title:Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions.
Authors:Hébert M,  Petiot P,  Benoit E,  Dansereau J,  Ahmad T,  Le Roch A,  Ottenwaelder X,  Gagnon A
Link:https://www.ncbi.nlm.nih.gov/pubmed/27231755?dopt=Abstract
Category:J Org Chem
PMID:27231755
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]