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1
A new approach to kainoids through tandem Michael reaction methodology: application to the enantioselective synthesis of (+)- and (-)-.alpha.-allokainic acid and to the formal synthesis of (-)-.alpha.-kainic acid
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A new approach to kainoids through tandem Michael reaction methodology: application to the enantioselective synthesis of (+)- and (-)-.alpha.-allokainic acid and to the formal synthesis of (-)-.alpha.-kainic acid

Barco, Achille ; Benetti, Simonetta ; Spalluto, Giampiero ; Casolari, Alberto ; Pollini, Gian P. ; Zanirato, Vinicio

Journal of organic chemistry, 1992-11, Vol.57 (23), p.6279-6286 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Reactivity of aryl and heteroaryl azides with vinylsilane and alkynylsilane. Formation of C-silylated 1,2,3-triazolines and 1,2,3-triazoles
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Reactivity of aryl and heteroaryl azides with vinylsilane and alkynylsilane. Formation of C-silylated 1,2,3-triazolines and 1,2,3-triazoles

ZANIRATO, P

Journal of the Chemical Society, Perkin Transactions 1, 1991 (11), p.2789-2796 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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3
A NEW APPROACH TO KAINOIDS THROUGH TANDEM MICHAEL REACTION METHODOLOGY - APPLICATION TO THE ENANTIOSELECTIVE SYNTHESIS OF (+)-ALPHA-ALLOKAINIC AND (-)-ALPHA-ALLOKAINIC ACID AND TO THE FORMAL SYNTHESIS OF (-)-ALPHA-KAINIC ACID
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A NEW APPROACH TO KAINOIDS THROUGH TANDEM MICHAEL REACTION METHODOLOGY - APPLICATION TO THE ENANTIOSELECTIVE SYNTHESIS OF (+)-ALPHA-ALLOKAINIC AND (-)-ALPHA-ALLOKAINIC ACID AND TO THE FORMAL SYNTHESIS OF (-)-ALPHA-KAINIC ACID

BARCO, A ; BENETTI, S ; SPALLUTO, G ; CASOLARI, A ; POLLINI, GP ; ZANIRATO

Journal of organic chemistry, 1992-11, Vol.57 (23), p.6279-6286 [Periódico revisado por pares]

WASHINGTON: Amer Chemical Soc

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4
Generation and cycloaddition reactions of 3-substituted-2-nitro-1,3-dienes
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Generation and cycloaddition reactions of 3-substituted-2-nitro-1,3-dienes

Barco, Achille ; Benetti, Simonetta ; Pollini, Gian P. ; Spalluto, Giampiero ; Zanirato, Vinicio

Tetrahedron letters, 1991-11, Vol.32 (22), p.2517-2520 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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5
Reactions of boranes with aromatic azides: III. A simple route to 1,2-dihydro- N-phenyl,thieno[ b]- and thieno[ c]-[1,2]azaborines
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Reactions of boranes with aromatic azides: III. A simple route to 1,2-dihydro- N-phenyl,thieno[ b]- and thieno[ c]-[1,2]azaborines

Zanirato, Paolo

Journal of organometallic chemistry, 1985-09, Vol.293 (3), p.285-293 [Periódico revisado por pares]

Lausanne: Elsevier B.V

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6
Reactions of boranes with aromatic azides
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Reactions of boranes with aromatic azides

Zanirato, Paolo

Journal of organometallic chemistry, 1985-09, Vol.293 (3), p.285-293 [Periódico revisado por pares]

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7
A convenient synthesis of γ-oxo-acrylates
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A convenient synthesis of γ-oxo-acrylates

MANFREDINI, S ; SIMONI, D ; ZANIRATO, V ; CASOLARI, A

Tetrahedron letters, 1988, Vol.29 (32), p.3997-4000 [Periódico revisado por pares]

Oxford: Elsevier

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8
Synthesis and reactivity of a stable precursor of 2-cyano-1,3-butadiene
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Synthesis and reactivity of a stable precursor of 2-cyano-1,3-butadiene

Baraldi, Pier Giovanni ; Barco, Achille ; Benetti, Simonetta ; Manfredini, Stefano ; Pollini, Gian Piero ; Simoni, Daniele ; Zanirato, Vinicio

Tetrahedron, 1988, Vol.44 (20), p.6451-6454 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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9
Synthetic studies towards forskolin
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Synthetic studies towards forskolin

Baraldi, P.G. ; Barco, A. ; Benetti, S. ; Ferretti, V. ; Pollini, G.P. ; Polo, E. ; Zanirato, V.

Tetrahedron, 1989, Vol.45 (5), p.1517-1532 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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10
Regio - and enantioselective bioreduction of ethyl 2,4-dioxoalkanoates and γ-Keto-α-enamino esters with fermenting baker's yeast
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Regio - and enantioselective bioreduction of ethyl 2,4-dioxoalkanoates and γ-Keto-α-enamino esters with fermenting baker's yeast

Baraldi, Pier G. ; Manfredini, Stefano ; Pollini, Gian P. ; Romagnoli, Romeo ; Simoni, Daniele ; Zanirato, Vinicio

Tetrahedron letters, 1992-05, Vol.33 (20), p.2871-2874 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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