about
The Emergence of Quinone Methides in Asymmetric OrganocatalysisA General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst.Catalytic Asymmetric Reactions of 4-Substituted Indoles with Nitroethene: A Direct Entry to Ergot Alkaloid Structures.Reactions between organomagnesium reagents and nitroarenes: past, present, and future.Concise and stereocontrolled synthesis of pseudo-C2-symmetric diamino alcohols and triamines for use in HIV protease inhibitors.Nucleophilic Dearomatization of Pyridines under Enamine Catalysis: Regio-, Diastereo-, and Enantioselective Addition of Aldehydes to Activated N-Alkylpyridinium Salts.Bioinspired organocatalytic asymmetric reactions.An organocatalytic enantioselective direct α-heteroarylation of aldehydes with isoquinoline N-oxides.Quinone-Fused Pyrazoles through 1,3-Dipolar Cycloadditions: Synthesis of Tricyclic Scaffolds and in vitro Cytotoxic Activity Evaluation on Glioblastoma Cancer CellsOrganocatalytic Asymmetric Conjugate Additions to Cyclopent-1-enecarbaldehyde: A Critical Assessment of Organocatalytic Approaches towards the Telaprevir Bicyclic CoreCatalytic asymmetric addition of Meldrum's acid, malononitrile, and 1,3-dicarbonyls to ortho-quinone methides generated in situ under basic conditionsAsymmetric synthesis of 3,4-annulated indoles through an organocatalytic cascade approachCatalytic highly enantioselective vinylogous Povarov reactionAn easy entry to optically active alpha-amino phosphonic acid derivatives using phase-transfer catalysis (PTC)Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl)Synthesis of alpha-hydrazino ketones via regio- and stereoselective electrophilic amination of manganese enolates and enaminesOrganocatalyzed solvent-free aza-Henry reaction: a breakthrough in the one-pot synthesis of 1,2-diaminesConformational studies by dynamic NMR. 72. Stereolabile enantiomers of acyl and thioacyl ferrocenesOrganocatalyzed Enantioselective Synthesis of Nitroalkanes Bearing All-Carbon Quaternary Stereogenic Centers through Conjugate Addition of Acetone CyanohydrinOrganocatalysis in the Asymmetric Synthesis of Nitrogen-Containing Compounds: How and WhyOrganocatalytic asymmetric aza-Michael reaction: enantioselective addition of O-benzylhydroxylamine to chalconesOrganocatalytic Enantioselective Decarboxylative Addition of Malonic Half Thioesters to IminesFirst 1,3-Dipolar Cycloaddition of Azomethine Ylides with (E)-Ethyl 3-Fluoroacrylate: Regio- and Stereoselective Synthesis of Enantiopure Fluorinated ProlinesTowards the Synthesis of Highly Functionalized Chiral α-Amino Nitriles by Aminative Cyanation and Their Synthetic ApplicationsChiral oxazoline-1,3-dithianes: new effective nitrogen–sulfur donating ligands in asymmetric catalysisRegiocontrolled Synthesis of Ring-Fused Thieno[2,3-c]pyrazoles through 1,3-Dipolar Cycloaddition of Nitrile Imines with Sulfur-Based AcetylenesSynthesis and reactivity of achiral and of a novel planar chiral thioferrocenoylsilanesSilylcupration of acylimidazolides: a new synthesis of α-aminoacylsilanes and their synthetic applicationsExtremely facile formation and high reactivity of new thioacylsilanes containing the ferrocene moietyStereoselective Three-Carbon and Two-Carbon Elongation of the Carbon Chain inN-Boc-Protected α-Aminoacylsilanes: An Entry to Functionalized β-Amino Alcohols and to Statine AnaloguesNew chiral allylaminosilanes and their use in asymmetric Sakurai reactionsCatalytic highly enantioselective transfer hydrogenation of β-trifluoromethyl nitroalkenes. An easy and general entry to optically active β-trifluoromethyl aminesCentral-to-Axial Chirality Conversion Approach Designed on Organocatalytic Enantioselective Povarov Cycloadditions: First Access to Configurationally Stable Indole-Quinoline Atropisomers
P50
Q28082249-62F9CD16-5CB7-444A-9E1A-9C98C8482F7BQ39533886-DBFF86AC-17E1-48BF-B710-D539B4E6A14BQ40214288-8872BCC1-C15E-46B7-8097-BC6F7AEEA13AQ40593767-B2D4FBB7-DC4E-492B-A133-49B3CD449155Q44314445-6ACB28A6-9B6D-4F52-858B-568F968563C8Q53809539-6E9AA082-B213-4851-BE20-ADC0E91F5682Q54344629-D33B02F9-DDA3-4140-9CD9-3A8470E6E2BAQ54622483-F0CF9C55-494A-4587-A8F2-3843B0A11FFCQ56373614-EC5FC48F-C7C8-4957-989E-B0D1C4CE38B9Q56967107-958FE904-68FB-4868-9338-D45A307B83ADQ56970411-5EA29809-B5FE-49C1-B73E-36A12E85E816Q56975694-58C50CEF-BA01-4F2A-A1CE-A7490002C7F8Q56979233-9D81BD65-FF25-4E0F-9538-1EE1F6EA992DQ56992424-3DC728CD-4EDC-42AB-82CC-993D3F13256FQ56996209-A0782798-65FB-4ADC-A491-AB5F1E222F60Q57001058-197A73B5-F9FD-472E-8562-19FB2AE28B9AQ57001089-4C166C4F-3742-4F56-BCAC-4EB9BEDDC3D4Q57010468-2AB89387-8E34-4A26-92FF-B93A2D01A094Q57539436-C8836D8D-5B03-44F3-8A4B-402DC5884DD9Q57539438-93833112-2444-4D59-A5DE-9CE939C00713Q57539440-29EFB6F8-432D-4016-8947-16333A1DA8A2Q57539444-03EDC349-63DF-4416-A7FA-F0F099353BBAQ57539451-E9718667-36BE-4030-89A3-57DD888C5685Q57539458-E03AACBB-FFDE-4DC5-91B1-FFFCB91F24BEQ57539459-ACC2F65C-552A-42F4-8F05-F9361C32A863Q58237143-D946C3AA-47CC-4421-BA5A-D54388CAC14CQ59647596-8B8019D6-5103-4B8D-AF9C-254E01EA2A1BQ59647606-2B7824ED-058B-4280-B457-91DEC7E92335Q59647608-763A029A-A952-47BE-908C-DB534A1A4A72Q59647609-C3909055-D2A1-40EA-94A7-4B40FE56B655Q59647611-F3C064E2-E993-4E1B-AA2F-148C88C0A71DQ86036162-A7F98514-BAAF-4ABD-A2AC-36394422FE5BQ90297890-200106ED-9922-446D-98CA-BB3226631F60
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mariafrancesca Fochi
@ast
Mariafrancesca Fochi
@en
Mariafrancesca Fochi
@es
Mariafrancesca Fochi
@nl
type
label
Mariafrancesca Fochi
@ast
Mariafrancesca Fochi
@en
Mariafrancesca Fochi
@es
Mariafrancesca Fochi
@nl
prefLabel
Mariafrancesca Fochi
@ast
Mariafrancesca Fochi
@en
Mariafrancesca Fochi
@es
Mariafrancesca Fochi
@nl
P106
P1153
6701651383
P31
P496
0000-0001-9124-3304