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1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes
1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes
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1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes

Baricordi, Nikla ; Benetti, Simonetta ; Bertolasi, Valerio ; De Risi, Carmela ; Pollini, Gian P. ; Zamberlan, Francesco ; Zanirato, Vinicio

Tetrahedron, 2012-01, Vol.68 (1), p.208-213 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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2
Hagemann's ester: a timeless building block for natural product synthesis
Hagemann's ester: a timeless building block for natural product synthesis
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Hagemann's ester: a timeless building block for natural product synthesis

Pollini, Gian Piero ; Benetti, Simonetta ; De Risi, Carmela ; Zanirato, Vinicio

Tetrahedron, 2010-04, Vol.66 (15), p.2775-2802 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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3
Synthesis of biomimetic light-driven molecular switches via a cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction
Synthesis of biomimetic light-driven molecular switches via a cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction
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Synthesis of biomimetic light-driven molecular switches via a cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction

Zanirato, Vinicio ; Pollini, Gian P. ; De Risi, Carmela ; Valente, Filippo ; Melloni, Alfonso ; Fusi, Stefania ; Barbetti, Jacopo ; Olivucci, Massimo

Tetrahedron, 2007-06, Vol.63 (23), p.4975-4982 [Periódico revisado por pares]

Elsevier Ltd

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4
A new enantiodivergent synthesis of the Geissman–Waiss lactone
A new enantiodivergent synthesis of the Geissman–Waiss lactone
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A new enantiodivergent synthesis of the Geissman–Waiss lactone

Barco, Achille ; Baricordi, Nikla ; Benetti, Simonetta ; De Risi, Carmela ; Pollini, Gian P. ; Zanirato, Vinicio

Tetrahedron, 2007-05, Vol.63 (20), p.4278-4283 [Periódico revisado por pares]

Elsevier Ltd

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5
From (−)-quinic acid to 8-azabicyclo[3.2.1]octane framework: Preparation of an enantiopure tropan-6α-ol
From (−)-quinic acid to 8-azabicyclo[3.2.1]octane framework: Preparation of an enantiopure tropan-6α-ol
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From (−)-quinic acid to 8-azabicyclo[3.2.1]octane framework: Preparation of an enantiopure tropan-6α-ol

Barco, Achille ; Benetti, Simonetta ; De Risi, Carmela ; Marchetti, Paolo ; Pollini, Gian P ; Zanirato, Vinicio

Tetrahedron, 1999-04, Vol.55 (18), p.5923-5930 [Periódico revisado por pares]

Elsevier Ltd

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6
Enantioselective synthesis of (−)-meroquinene through tandem Michael reaction methodology
Enantioselective synthesis of (−)-meroquinene through tandem Michael reaction methodology
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Enantioselective synthesis of (−)-meroquinene through tandem Michael reaction methodology

Barco, Achille ; Benetti, Simonetta ; Risi, Carmela De ; Pollini, Gian P. ; Romagnoli, Romeo ; Spalluto, Giampiero ; Zanirato, Vinicio

Tetrahedron, 1994-02, Vol.50 (8), p.2583-2590 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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7
A [3+2]nitrile oxide cycloaddition approach to (−)-pyrenophorin, and rosefuran
A [3+2]nitrile oxide cycloaddition approach to (−)-pyrenophorin, and rosefuran
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A [3+2]nitrile oxide cycloaddition approach to (−)-pyrenophorin, and rosefuran

Barco, Achille ; Benetti, Simonetta ; Risi, Carmela De ; Pollini, Gian P. ; Zanirato, Vinicio

Tetrahedron, 1995-07, Vol.51 (28), p.7721-7726 [Periódico revisado por pares]

Elsevier Ltd

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8
Generation and cycloaddition reactions of substituted 2-nitro-1,3-dienes
Generation and cycloaddition reactions of substituted 2-nitro-1,3-dienes
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Generation and cycloaddition reactions of substituted 2-nitro-1,3-dienes

Barco, Achille ; Benetti, Simonetta ; De Risi, Carmela ; Morelli, Carlo F. ; Pollini, Gian P. ; Zanirato, Vinicio

Tetrahedron, 1996-07, Vol.52 (27), p.9275-9288 [Periódico revisado por pares]

Elsevier Ltd

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9
4-Isopropyl-2-oxazolin-5-one anion as masked umpoled synthon for both formyl and hydroxycarbonyl anions: Generation, reactivity and synthetic applications
4-Isopropyl-2-oxazolin-5-one anion as masked umpoled synthon for both formyl and hydroxycarbonyl anions: Generation, reactivity and synthetic applications
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4-Isopropyl-2-oxazolin-5-one anion as masked umpoled synthon for both formyl and hydroxycarbonyl anions: Generation, reactivity and synthetic applications

Barco, Achille ; Benetti, Simonetta ; De Risi, Carmela ; Pollini, Gian P ; Spalluto, Giampiero ; Zanirato, Vinicio

Tetrahedron, 1996-03, Vol.52 (13), p.4719-4734 [Periódico revisado por pares]

Elsevier Ltd

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10
A unified asymmetric approach to substituted hexahydroazepine and 7-azabicyclo[2.2.1]heptane ring systems from D(−)-quinic acid: Application to the formal synthesis of (−)-balanol and (−)-epibatidine
A unified asymmetric approach to substituted hexahydroazepine and 7-azabicyclo[2.2.1]heptane ring systems from D(−)-quinic acid: Application to the formal synthesis of (−)-balanol and (−)-epibatidine
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A unified asymmetric approach to substituted hexahydroazepine and 7-azabicyclo[2.2.1]heptane ring systems from D(−)-quinic acid: Application to the formal synthesis of (−)-balanol and (−)-epibatidine

Albertini, Enrichetta ; Barco, Achille ; Benetti, Simonetta ; De Risi, Carmela ; Pollini, Gian P ; Zanirato, Vinicio

Tetrahedron, 1997-12, Vol.53 (50), p.17177-17194 [Periódico revisado por pares]

Elsevier Ltd

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