Stebėti
Mihaela Gulea
Mihaela Gulea
Patvirtintas el. paštas unistra.fr
Pavadinimas
Cituota
Cituota
Metai
Recent advances in the chemistry of organic thiocyanates
T Castanheiro, J Suffert, M Donnard, M Gulea
Chemical Society Reviews 45 (3), 494-505, 2016
2802016
Overview of the chemistry of 2-thiazolines
AC Gaumont, M Gulea, J Levillain
Chemical reviews 109 (3), 1371-1401, 2009
2192009
Mercaptophosphonate compounds as broad-spectrum inhibitors of the metallo-β-lactamases
P Lassaux, M Hamel, M Gulea, H Delbrück, PS Mercuri, L Horsfall, ...
Journal of medicinal chemistry 53 (13), 4862-4876, 2010
1632010
Synthesis and properties of thiazoline based ionic liquids derived from the chiral pool
J Levillain, G Dubant, I Abrunhosa, M Gulea, AC Gaumont
Chemical communications, 2914-2915, 2003
1242003
Chiral thiazoline ligands: application in Pd-catalysed allylic substitution
I Abrunhosa, L Delain-Bioton, AC Gaumont, M Gulea, S Masson
Tetrahedron 60 (41), 9263-9272, 2004
822004
Synthesis of new chiral thiazoline-containing ligands
I Abrunhosa, M Gulea, J Levillain, S Masson
Tetrahedron: Asymmetry 12 (20), 2851-2859, 2001
752001
5-Endo-Trig Radical Cyclizations of Bromomethyldimethylsilyl Diisopropylpropargylic Ethers. A Highly Diastereoselective Access to Functionalized Cyclopentanes
S Bogen, M Gulea, L Fensterbank, M Malacria
The Journal of Organic Chemistry 64 (13), 4920-4925, 1999
751999
Recent contributions to hetero Diels-Alder reactions
G Blond, M Gulea, V Mamane
Current Organic Chemistry 20 (21), 2161-2210, 2016
722016
Cyclocarbopalladation/Cross-coupling cascade reactions in sulfide series: Access to sulfur heterocycles
T Castanheiro, M Donnard, M Gulea, J Suffert
Organic letters 16 (11), 3060-3063, 2014
602014
Synthesis of medium-sized heterocycles by transition-metal-catalyzed intramolecular cyclization
M Choury, A Basilio Lopes, G Blond, M Gulea
Molecules 25 (14), 3147, 2020
552020
1, 4-Hydrogen radical transfer as a new and versatile tool for the synthesis of enantiomerically pure 1, 2, 3-triols
M Gulea, JM López-Romero, L Fensterbank, M Malacria
Organic Letters 2 (17), 2591-2594, 2000
512000
Pyridinedithioesters as heterodienophiles: application to the synthesis of aprikalim
R Bastin, H Albadri, AC Gaumont, M Gulea
Organic letters 8 (6), 1033-1036, 2006
492006
Ruthenium–porphyrin-catalyzed carbenoid addition to allylic compounds: application to [2, 3]-sigmatropic rearrangements of ylides
G Simonneaux, E Galardon, C Paul-Roth, M Gulea, S Masson
Journal of Organometallic Chemistry 617, 360-363, 2001
422001
Practical access to aromatic thiocyanates by CuCN‐mediated direct aerobic oxidative cyanation of thiophenols and diaryl disulfides
T Castanheiro, M Gulea, M Donnard, J Suffert
European Journal of Organic Chemistry 2014 (35), 7814-7817, 2014
412014
Cyclopropanation of alkenes with diisopropyl diazomethylphosphonate catalysed by ruthenium porphyrin complexes
C Paul-Roth, F De Montigny, G Rethoré, G Simonneaux, M Gulea, ...
Journal of Molecular Catalysis A: Chemical 201 (1-2), 79-91, 2003
412003
First catalytic enantioselective version of a thia hetero-Diels–Alder reaction with dithioesters
H Dentel, I Chataigner, F Le Cavelier, M Gulea
Tetrahedron Letters 51 (46), 6014-6017, 2010
372010
Synthesis of chiral, nonracemic α-sulfanylphosphonates and derivatives
M Gulea, F Hammerschmidt, P Marchand, S Masson, V Pisljagic, ...
Tetrahedron: Asymmetry 14 (13), 1829-1836, 2003
372003
2 Sigmatropic [2,3]-Wittig rearrangement of the α-allylic-heterosubstituted methylphosphonates. Part 3: High diastereoselectivity in the rearrangement of anion of dimenthyl …
M Gulea-Purcarescu, E About-Jaudet, N Collignon
Tetrahedron Lett., 1995
371995
Cyclocarbopalladation as a key step in cascade reactions: Recent developments
S Blouin, G Blond, M Donnard, M Gulea, J Suffert
Synthesis 49 (08), 1767-1784, 2017
362017
Application of chiral 2, 6-bis (thiazolinyl) pyridines in asymmetric Ru-catalyzed cyclopropanations with diazoesters
P Le Maux, I Abrunhosa, M Berchel, G Simonneaux, M Gulea, S Masson
Tetrahedron: Asymmetry 15 (16), 2569-2573, 2004
362004
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