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Marina Porcelloni
Observed names:
M. PORCELLONI,
Porcelloni, Marina
Institution:
Menarini Group (Italy)
Observed institutions:
University of Bristol,
Menarini Group (Italy),
University of Florence,
University of Sheffield
OpenAlex ID:
A5082985642
Application of Chiral Sulfides to Catalytic Asymmetric Aziridination and Cyclopropanation with In Situ Generation of the Diazo Compound
2001
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
Angewandte Chemie International Edition
·
377
Histone Deacetylase Inhibitors: From Bench to Clinic
2008
·
Marielle Paris
, Marina Porcelloni
, et al.
·
Journal of Medicinal Chemistry
·
373
Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with In Situ Generation of Diazocompounds
2001
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
Angewandte Chemie International Edition
·
217
PDF
A New Protocol for the In Situ Generation of Aromatic, Heteroaromatic, and Unsaturated Diazo Compounds and Its Application in Catalytic and Asymmetric Epoxidation of Carbonyl Compounds. Extensive Studies To Map Out Scope and Limitations, and Rationalization of Diastereo- and Enantioselectivities
2003
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
Journal of the American Chemical Society
·
191
Verwendung chiraler Sulfide zur katalytischen asymmetrischen Aziridinierung und Cyclopropanierung mit in situ gebildeter Diazokomponente
2001
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
Angewandte Chemie
·
89
Katalytische asymmetrische Epoxidierung von Aldehyden mit Schwefel-Yliden und in situ hergestellten Diazoverbindungen
2001
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
Angewandte Chemie
·
49
A New Palladium-Catalyzed Intramolecular Allylation to Pyrrolidin-2-ones 1
1998
·
Giuliano Giambastiani
, Barbara Pacini
, et al.
·
The Journal of Organic Chemistry
·
46
hNK2 receptor antagonists. The use of intramolecular hydrogen bonding to increase solubility and membrane permeability
2011
·
Alessandro Ettorre
, Piero D’Andrea
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
36
Effect of sulfide structure on enantioselectivity in catalytic asymmetric epoxidation of aldehydes: Mechanistic insights and implications
2004
·
Varinder K. Aggarwal
, Jonathan Charmant
, et al.
·
Proceedings of the National Academy of Sciences
·
34
Alkyl piperidine and piperazine hydroxamic acids as HDAC inhibitors
2011
·
Cristina Rossi
, Marina Porcelloni
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
23
Histone Deacetylase Inhibitors: From Bench to Clinic
2008
·
Marielle Paris
, Marina Porcelloni
, et al.
·
Journal of Medicinal Chemistry
·
21
Structure−Activity Relationships of 6-Methyl-benzo[b]thiophene-2-carboxylic Acid (1-{(S)-1-Benzyl-4-[4-(tetrahydropyran-4-ylmethyl)piperazin-1-yl]butylcarbamoyl}cyclopentyl)amide, Potent Antagonist of the Neurokinin-2 Receptor
2010
·
Daniela Fattori
, Marina Porcelloni
, et al.
·
Journal of Medicinal Chemistry
·
15
Solid-phase synthesis of unsymmetrical ureas through the use of Kenner safety-catch linker
2003
·
Daniela Fattori
, Piero D'Andrea
, et al.
·
Tetrahedron Letters
·
12
Benzofused hydroxamic acids: Useful fragments for the preparation of histone deacetylase inhibitors. Part 1: Hit identification
2013
·
Elena Marastoni
, Sandra Bartoli
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
10
α,α‐Cyclopentaneglycine Dipeptides Capped with Biaryls as Tachykinin NK2 Receptor Antagonists
2008
·
Marina Porcelloni
, Piero D'Andrea
, et al.
·
ChemMedChem
·
10
Benzofused hydroxamic acids: Useful fragments for the preparation of histone deacetylase inhibitors. Part 2: 7-Fluorobenzothiophenes and benzofurans
2015
·
Elena Marastoni
, Sandra Bartoli
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
7
4-N-Hydroxy-4-[1-(sulfonyl)piperidin-4-yl]-butyramides as HDAC inhibitors
2011
·
Cristina Rossi
, Christopher I. Fincham
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
6
Generation of a new class of hNK2 receptor ligands using the ‘fragment approach’
2004
·
Piero D’Andrea
, Marina Porcelloni
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
6
Cinnamic acids and mono-substituted benzoic acids as useful capping groups for the preparation of hNK2 receptor antagonists
2008
·
Marina Porcelloni
, Piero D’Andrea
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
4
ChemInform Abstract: Histone Deacetylase Inhibitors: From Bench to Clinic
2008
·
Marielle Paris
, Marina Porcelloni
, et al.
·
ChemInform
·
3
CCDC 1044933: Experimental Crystal Structure Determination
2015
·
Marastoni, Elena
, Bartoli, Sandra
, et al.
·
The Cambridge Structural Database
Generation of a New Class of hNK2 Receptor Ligands Using the ′Fragment Approach′.
2005
·
Piero D'Andrea
, Marina Porcelloni
, et al.
·
ChemInform
ChemInform Abstract: Application of Chiral Sulfides to Catalytic Asymmetric Aziridination and Cyclopropanation with in situ Generation of the Diazo Compound.
2001
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
ChemInform
ChemInform Abstract: Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with in situ Generation of Diazocompounds.
2001
·
Varinder K. Aggarwal
, Emma Alonso
, et al.
·
ChemInform
ChemInform Abstract: A New Palladium‐Catalyzed Intramolecular Allylation to Pyrrolidin‐2‐ones.
1998
·
G. GIAMBASTIANI
, B. PACINI
, et al.
·
ChemInform
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Works count:
25
Citation count:
1,529
H-index:
12
I10-index:
15
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