Claudia Lalli
Overview
Explore the profile of Claudia Lalli including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
24
Citations
121
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Le Roch M, Gouault N, Renault J, Argouarch G, Roisnel T, Banik S, et al.
Org Biomol Chem
. 2025 Jan;
23(7):1644-1652.
PMID: 39775693
A straightforward and highly diastereoselective synthesis of -4-hydroxypiperidines is presented. This method allows access to C2 and C4 substituted piperidines, bearing a tetrasubstituted carbon stereocenter at C4. -Disubstituted homoallylic amines...
2.
Martel A, Zaier R, Braire J, Mace A, Vidal J, Lalli C, et al.
J Org Chem
. 2024 Sep;
89(18):13224-13234.
PMID: 39258765
Allylboration reactions of ketones catalyzed by BINOL derivatives can exhibit highly variable stereochemical courses depending on the nature and reactivity of the ketone substrate. In this Article, we put into...
3.
Le Roch M, Renault J, Argouarch G, Lenci E, Trabocchi A, Roisnel T, et al.
J Org Chem
. 2024 Mar;
89(7):4932-4946.
PMID: 38451837
The concise synthesis of a small library of fluorinated piperidines from readily available dihydropyridinone derivatives has been described. The effect of the fluorination on different positions has then been evaluated...
4.
Gantasala N, Fournet C, Le Roch M, Lalli C, Pabbaraja S, Gouault N
Org Biomol Chem
. 2023 Jun;
21(25):5245-5253.
PMID: 37306584
A novel approach to build 2-spiropiperidine moieties starting from dihydropyridones was developed. The triflic anhydride-promoted conjugate addition of allyltributylstannane onto dihydropyridones allowed for the formation of bis-alkenyl intermediates that were...
5.
Mattei C, Montigaud V, Lefeuvre B, Dorcet V, Argouarch G, Cador O, et al.
J Mater Chem C Mater
. 2023 Jun;
11(22):7299-7310.
PMID: 37304727
Lanthanide ions have attracted great interest owing to their optical and magnetic properties. Single-molecule magnet (SMM) behavior has been a fascinating science for thirty years. Moreover, chiral lanthanide complexes allow...
6.
Braire J, Mace A, Zaier R, Cordier M, Vidal J, Lalli C, et al.
J Org Chem
. 2023 Jan;
88(3):1469-1492.
PMID: 36690446
An improvement in the catalytic enantioselective allylboration of isatins with 2-allyl-1,3,2-dioxaborolane in the presence of chiral BINOL derivatives is reported, offering an efficient one-step access to enantioenriched -unprotected 3-allyl-3-hydroxy-2-oxindoles. This...
7.
Sun Y, Dhbaibi K, Lauwick H, Lalli C, Taupier G, Molard Y, et al.
Chemistry
. 2022 Nov;
29(10):e202203243.
PMID: 36367394
A novel enantiopure π-allylruthenium(IV) precatalyst allowed the enantioselective and stereospecific allylations of indoles and gave access to indolin-3-ones, containing vicinal stereogenic centers. Facile separation of diastereoisomers exhibiting opposite circularly polarized...
8.
Mattei C, Dhbaibi K, Lefeuvre B, Dorcet V, Argouarch G, Cador O, et al.
Chirality
. 2021 Nov;
34(1):34-47.
PMID: 34750861
The interest for lanthanide circularly polarized luminescence (CPL) has been quickly growing for 10 years. However, very few of these studies have involved correlation between the dissymmetry factor (g )...
9.
Lefeuvre B, Mattei C, Gonzalez J, Gendron F, Dorcet V, Riobe F, et al.
Chemistry
. 2021 Mar;
27(26):7362-7366.
PMID: 33780055
A field-induced chiral Yb Single-Molecule Magnet (SMM) displayed an unprecedented near-infrared circularly polarized luminescence (NIR-CPL) in the solid-state. The bridging bis(1,10-phenantro[5,6b])tetrathiafulvalene triad (L) allowed an efficient sensitization of the NIR...
10.
Vu T, Delalande O, Lalli C, Reider S, Ferron S, Boustie J, et al.
Planta Med
. 2021 Feb;
87(9):701-708.
PMID: 33618379
Protein tyrosine phosphatase 1B plays a significant role in type 2 diabetes mellitus and other diseases and is therefore considered a new drug target. Within this study, an acetone extract...