BRENNA, DAVIDE

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BRENNA, DAVIDE

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Dipartimento di Chimica

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Risultati 1 - 13 di 13 (tempo di esecuzione: 0.013 secondi).

2-Carboxythioester-1,3-dithiane: a functionalized masked carbonyl nucleophile for the organocatalytic enantioselective Michael addition to enones

2016 E. Massolo, D. Brenna, F. Cozzi, L. Raimondi, N. Gaggero, M. Benaglia

A new class of low-loading catalysts for a highly enantioselective, metal-free imine reduction of wide general applicability

2017 D. Brenna, R. Porta, E. Massolo, L. Raimondi, M. Benaglia

A stereoselective, catalytic strategy for the in-flow synthesis of advanced precursors of Rasagiline and Tamsulosin

2017 D. Brenna, M. Pirola, L. Raimondi, A.J. Burke, M. Benaglia

HSiCl3 mediated synthesis of rivastigmine and miotine

2015 D. Brenna, M. Benaglia

Hydrogen borrowing mediated, iron catalyzed, functionalization of Α,Β unsatured alcohols

2016 D. Brenna, M. Benaglia

In-flow synthesis of advanced precursors of Chiral APIs

2017 M. Pirola, D. Brenna, L.M. Raimondi, A.J. Burke, M. Benaglia

Iron catalyzed diastereoselective hydrogenation of chiral imines

2017 D. Brenna, S. Rossi, F. Cozzi, M. Benaglia

Recent developments in the reduction of aromatic and aliphatic nitro compounds to amines

2018 M. Orlandi, D. Brenna, R. Harms, S. Jost, M. Benaglia

Stereoselective Catalytic Synthesis of Active Pharmaceutical Ingredients in Homemade 3D-Printed Mesoreactors

2017 S. Rossi, R. Porta, D. Brenna, A. Puglisi, M. Benaglia

Stereoselective metal-free reduction of chiral imines in batch and in flow mode. A convenient strategy for the synthesis of chiral Active Pharmaceutical Ingredients

2017 D. Brenna, M. Benaglia, R. Porta, S.D. Fernandes, A.J. Burke

SUSTAINABLE PREPARATION OF APIS IN BATCH&FLOW MODE, AND IRON CATALYZED TRANSFORMATIONS

2018 D. Brenna

Synthesis of highly decorated chiral 2-nitro-cyclohexane carboxylic esters through microwave-assisted organocatalyzed cascade reactions

2014 E. Massolo, M. Benaglia, D. Parravicini, D. Brenna, R. Annunziata

Towards the development of continuous, organocatalytic, and stereoselective reactions in deep eutectic solvents

2016 D. Brenna, E. Massolo, A. Puglisi, S. Rossi, G. Celentano, M. Benaglia, V. Capriati

Titolo	Data di pubblicazione	Autori	Tipo	Abstract
2-Carboxythioester-1,3-dithiane: a functionalized masked carbonyl nucleophile for the organocatalytic enantioselective Michael addition to enones	1-gen-2016	E. MassoloD. BrennaF. CozziL. RaimondiN. GaggeroM. Benaglia	Article (author)	-
A new class of low-loading catalysts for a highly enantioselective, metal-free imine reduction of wide general applicability	1-mar-2017	D. BrennaR. PortaE. MassoloL. RaimondiM. Benaglia	Article (author)	-
A stereoselective, catalytic strategy for the in-flow synthesis of advanced precursors of Rasagiline and Tamsulosin	1-dic-2017	D. BrennaM. PirolaL. RaimondiA. J. BurkeM. Benaglia + -	Article (author)	-
HSiCl3 mediated synthesis of rivastigmine and miotine	15-giu-2015	BRENNA, DAVIDEM. Benaglia	Conference Object	-
Hydrogen borrowing mediated, iron catalyzed, functionalization of Α,Β unsatured alcohols	13-giu-2016	D. BrennaM. Benaglia	Conference Object	-
In-flow synthesis of advanced precursors of Chiral APIs	22-giu-2017	Margherita PirolaDavide BrennaLaura RaimondiAnthony J. BurkeMaurizio Benaglia + -	Conference Object	-
Iron catalyzed diastereoselective hydrogenation of chiral imines	21-lug-2017	D. BrennaS. RossiF. CozziM. Benaglia	Article (author)	-
Recent developments in the reduction of aromatic and aliphatic nitro compounds to amines	20-apr-2018	M. OrlandiD. BrennaR. HarmsS. JostM. Benaglia + -	Article (author)	-
Stereoselective Catalytic Synthesis of Active Pharmaceutical Ingredients in Homemade 3D-Printed Mesoreactors	3-apr-2017	S. RossiR. PortaD. BrennaA. PuglisiM. Benaglia	Article (author)	-
Stereoselective metal-free reduction of chiral imines in batch and in flow mode. A convenient strategy for the synthesis of chiral Active Pharmaceutical Ingredients	1-gen-2017	D. BrennaM. BenagliaR. PortaS. D. FernandesA. J. Burke + -	Article (author)	-
SUSTAINABLE PREPARATION OF APIS IN BATCH&FLOW MODE, AND IRON CATALYZED TRANSFORMATIONS	1-feb-2018	BRENNA, DAVIDE	Doctoral Thesis	-
Synthesis of highly decorated chiral 2-nitro-cyclohexane carboxylic esters through microwave-assisted organocatalyzed cascade reactions	1-gen-2014	MASSOLO, ELISABETTAM. BenagliaD. ParraviciniD. BrennaANNUNZIATA, RITA MARIA + -	Article (author)	-
Towards the development of continuous, organocatalytic, and stereoselective reactions in deep eutectic solvents	1-gen-2016	D. BrennaE. MassoloA. PuglisiS. RossiG. CelentanoM. BenagliaV. Capriati + -	Article (author)	-

IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

BRENNA, DAVIDE

2-Carboxythioester-1,3-dithiane: a functionalized masked carbonyl nucleophile for the organocatalytic enantioselective Michael addition to enones

A new class of low-loading catalysts for a highly enantioselective, metal-free imine reduction of wide general applicability

A stereoselective, catalytic strategy for the in-flow synthesis of advanced precursors of Rasagiline and Tamsulosin

HSiCl3 mediated synthesis of rivastigmine and miotine

Hydrogen borrowing mediated, iron catalyzed, functionalization of Α,Β unsatured alcohols

In-flow synthesis of advanced precursors of Chiral APIs

Iron catalyzed diastereoselective hydrogenation of chiral imines

Recent developments in the reduction of aromatic and aliphatic nitro compounds to amines

Stereoselective Catalytic Synthesis of Active Pharmaceutical Ingredients in Homemade 3D-Printed Mesoreactors

Stereoselective metal-free reduction of chiral imines in batch and in flow mode. A convenient strategy for the synthesis of chiral Active Pharmaceutical Ingredients

SUSTAINABLE PREPARATION OF APIS IN BATCH&FLOW MODE, AND IRON CATALYZED TRANSFORMATIONS

Synthesis of highly decorated chiral 2-nitro-cyclohexane carboxylic esters through microwave-assisted organocatalyzed cascade reactions

Towards the development of continuous, organocatalytic, and stereoselective reactions in deep eutectic solvents