Margery Cortes-Clerget
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Explore the profile of Margery Cortes-Clerget including associated specialties, affiliations and a list of published articles.
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13
Citations
180
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Recent Articles
1.
Wu B, Ye N, Zhao K, Shi M, Liao J, Zhang J, et al.
Chem Commun (Camb)
. 2024 Jan;
60(17):2349-2352.
PMID: 38284323
A sustainable C(sp)-C(sp) cross-electrophile coupling was developed between readily available 5-bromophthalide and 1-benzyl-4-iodopiperidine under micellar conditions, leading to a key intermediate of one of our development compounds. Copper was found...
2.
Singhania V, Cortes-Clerget M, Dussart-Gautheret J, Akkachairin B, Yu J, Akporji N, et al.
Chem Sci
. 2022 Feb;
13(5):1440-1445.
PMID: 35222928
Esterification in an aqueous micellar medium is catalyzed by a commercially available lipase in the absence of any co-factors. The presence of only 2 wt% designer surfactant, TPGS-750-M, assists in...
3.
Ye N, Wu B, Zhao K, Ge X, Zheng Y, Shen X, et al.
Chem Commun (Camb)
. 2021 Jul;
57(62):7629-7632.
PMID: 34232240
A robust and sustainable C(sp2)-C(sp3) cross-electrophile coupling was developed via nickel/copper synergistic catalysis under micellar conditions. This protocol provided a general method to access alkylated arenes with good to excellent...
4.
Cortes-Clerget M, Yu J, Kincaid J, Walde P, Gallou F, Lipshutz B
Chem Sci
. 2021 Jun;
12(12):4237-4266.
PMID: 34163692
A review presenting water as the logical reaction medium for the future of organic chemistry. A discussion is offered that covers both the "on water" and "in water" phenomena, and...
5.
Akporji N, Thakore R, Cortes-Clerget M, Andersen J, Landstrom E, Aue D, et al.
Chem Sci
. 2021 Jun;
11(20):5205-5212.
PMID: 34122976
A new biaryl phosphine-containing ligand from an active palladium catalyst for ppm level Suzuki-Miyaura couplings, enabled by an aqueous micellar reaction medium. A wide array of functionalized substrates including aryl/heteroaryl...
6.
Wood A, Cortes-Clerget M, Kincaid J, Akkachairin B, Singhania V, Gallou F, et al.
Angew Chem Int Ed Engl
. 2020 Jun;
59(40):17587-17593.
PMID: 32579762
Mild mono- and di-hydrodehalogenative reductions of gem-dibromocyclopropanes are described, providing an easy and green approach towards the synthesis of cyclopropanes. The methodology utilizes 0.5-5 mol % TMPhen-nickel as the catalyst,...
7.
Cortes-Clerget M, Akporji N, Zhou J, Gao F, Guo P, Parmentier M, et al.
Nat Commun
. 2019 May;
10(1):2169.
PMID: 31092815
Previous studies have shown that aqueous solutions of designer surfactants enable a wide variety of valuable transformations in synthetic organic chemistry. Since reactions take place within the inner hydrophobic cores...
8.
Cortes-Clerget M, Lee N, Lipshutz B
Nat Protoc
. 2019 Mar;
14(4):1108-1129.
PMID: 30903108
Amide bond formation and aromatic/heteroaromatic nitro-group reductions represent two of the most commonly used transformations in organic synthesis. Unfortunately, such processes can be especially wasteful and hence environmentally harmful, and...
9.
Lee N, Cortes-Clerget M, Wood A, Lippincott D, Pang H, Moghadam F, et al.
ChemSusChem
. 2019 Mar;
12(13):3159-3165.
PMID: 30889298
Several types of reduction reactions in organic synthesis are performed under aqueous micellar-catalysis conditions (in water at ambient temperature), which produce a significant volume of foam owing to the combination...
10.
Lipshutz B, Ghorai S, Cortes-Clerget M
Chemistry
. 2018 Feb;
24(26):6672-6695.
PMID: 29465785
Recent developments over the past few years in aqueous micellar catalysis are discussed. Applications to problems in synthesis are highlighted, enabled by the use of surfactants that self-aggregate in water...