Martina Gensini

Menarini Group (Italy)

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S.I. Kozhushkov

University of Göttingen

Alberto Brandi

University of Florence

A. de Meijere

University of Göttingen

Laura Quartara

Menarini Group (Italy)

Armin de Meijere

University of Göttingen

M. Es‐Sayed

Bayer (Germany)

Maria Maddalena Altamura

Sapienza University of Rome

Carlo Alberto Maggi

Menarini Group (Italy)

D. Vidovic

University of Zagreb

Rossano Nannicini

Menarini Group (Italy)

Cooperative Institutions

Menarini Group (Italy)

University of Florence

Sorain Cecchini Tecno (Italy)

University of Göttingen

Centre National de la Recherche Scientifique

Mario Negri Institute for Pharmacological Research

St Petersburg University

University of Iowa

Sapienza University of Rome

Istituti di Ricovero e Cura a Carattere Scientifico

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1,3-Dipolar Cycloadditions of 2-tert-Butoxycarbonyl-1-pyrroline N-Oxide with Chiral Acrylates and Acrylamides

Heterocycles (2006)

Alberto Brandi Federica Pisaneschi Martina Gensini Maria Salvati Franca M. Cordero

The 1,3-dipolar cycloadditions of a series of chiral acrylates and acrylamides with 2-tert-butoxycarbonyl-1-pyrroline N-oxide were studied.The synthesis of enantiopure tert-butyl (2R,7aR)-and (2S,7aS)-2-hydroxy-3-oxo-tetrahydro-1H-pyrrolizine-7a(5H)-carboxylates starting from the acryloyloxazolidinone derived from (S)-phenylalanine is reported.

Pyrroline

10.3987/com-05-s(t)37

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Citations (7)

Cyclopropyl Building Blocks in Organic Synthesis. Part 91. Di‐ and Trispirocyclopropanated Tetrahydropyridinones.

ChemInform (2003)

Martina Gensini S.I. Kozhushkov Daniel Frank D. Vidovic Alberto Brandi

10.1002/chin.200337121

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Citations (0)

CCDC 206103: Experimental Crystal Structure Determination

The Cambridge Structural Database (2004)

Martina Gensini A. De Meijere

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

10.5517/cc6xgh1

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Cyclopropyl Building Blocks for Organic Synthesis. Part 102. A Convenient New Synthesis of 3-Substituted ?-Lactams Formally Derived from 1-(Aminomethyl)cyclopropanecarboxylic Acids.

ChemInform (2005)

Alessandra Zanobini Martina Gensini J. Magull D. Vidovic S.I. Kozhushkov

Abstract For Abstract see ChemInform Abstract in Full Text.

Organic Synthesis

10.1002/chin.200505095

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Citations (1)

Cyclopropyl Building Blocks for Organic Synthesis. Part 94. Cyclopropane‐Anellated Azaoligoheterocycles by Ti‐Mediated Intramolecular Reductive Cyclopropanation of Cyclic Amino Acid Amides.

ChemInform (2004)

Martina Gensini Armin de Meijere

Cyclopropane

10.1002/chin.200425198

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CCDC 199270: Experimental Crystal Structure Determination

The Cambridge Structural Database (2003)

Martina Gensini S.I. Kozhushkov Douglas G. Frank D. Vidović A. Brandi

10.5517/cc6pc29

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Molecular Rearrangements: Part 2

Organic Reaction Mechanisms/Organic reaction mechanisms (2006)

Alberto Brandi Martina Gensini Federica Pisaneschi

This chapter contains sections titled: Aromatic Rearrangements Ionic Rearrangements Rearrangements Involving Organometallic Compounds Rearrangements Involving Ring Opening Isomerizations Tautomerism Radical Rearrangements References

10.1002/0470022051.ch14

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Stereodivergent Approach to Enantiopure Hydroxyindolizidines Through 1,3-Dipolar Cycloaddition of 3-Hydroxypyrroline N-Oxide Derivatives

European Journal of Organic Chemistry (2002)

Franca M. Cordero Federica Pisaneschi Martina Gensini Andrea Goti Alberto Brandi

Nitrone

Enantiopure drug

Moiety

Racemization

10.1002/1099-0690(200206)2002:12<1941::aid-ejoc1941>3.0.co;2-t

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Citations (54)

3‐Azabicyclo[3.1.0]hex‐1‐ylamines by Ti‐Mediated Intramolecular Reductive Cyclopropanation of α‐(N‐Allylamino)‐Substituted N,N‐Dialkylcarboxamides and Carbonitriles.

ChemInform (2002)

Martina Gensini S.I. Kozhushkov Dmitrii S. Yufit Judith A. K. Howard M. Es‐Sayed

Abstract For Abstract see ChemInform Abstract in Full Text.

Reductive elimination

10.1002/chin.200246051

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Solvent Dependent Benzylic Radical Bromination of Aromatic Sulfonyl Chlorides

Letters in Organic Chemistry (2006)

Laura Quartara Maria Maddalena Altamura Annalisa Guerri Rossano Nannicini Martina Gensini

We have studied the solvent dependent radical bromination of toluene sulfonyl chlorides. The use of acetonitrile allows to avoid chlorinated solvents and to improve the yield and the reproducibility of the process. Keywords: aromatic sulfonyl chloride, benzyl bromide, N-bromosuccinimide, Radical bromination

Sulfonyl

10.2174/157017806775789958

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Citations (3)