Zobrazeno 1 - 10 of 26 pro vyhledávání: '"Giada Moscatelli"'
1
Regioselective Formation of 5-Methylene-6-methoxy-1,4,5,6-tetrahydropyridazines from the [4+2]-Cycloaddition Reaction of In Situ Generated 1,2-Diaza-1,3-dienes with Methoxyallene
Autor: Simona Nicolini, Fabio Mantellini, Giada Moscatelli, Gianfranco Favi, Orazio A. Attanasi, Serena Mantenuto
Publikováno v: Synlett. 26:193-196
A regioselective inverse-electron-demand hetero-Diels–­Alder reaction of in situ generated 1,2-diaza-1,3-dienes with methoxyallene is reported. These Lewis and Bronsted acid free reactions benefit from operational simplicity and allow access to sy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c6e709117b37a323fc10891fc2fa7c5
https://doi.org/10.1055/s-0034-1379550
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2
Synthesis of Densely Functionalized 3a,4-Dihydro-1H-Pyrrolo[1,2-b]Pyrazoles via Base Mediated Domino Reaction of Vinyl Malononitriles with 1,2-Diaza-1,3-dienes
Autor: Fabio Mantellini, Giada Moscatelli, Gianfranco Favi, Orazio A. Attanasi, Aliki Paparisva, Athina Geronikaki
Publikováno v: Organic Letters. 15:2624-2627
A domino reaction of vinyl malononitriles (VMs) with 1,2-diaza-1,3-dienes (DDs) produce unprecedented 3a,4-dihydro-1H-pyrrolo[1,2-b]pyrazole systems in a chemo-, regio-, and stereoselective fashion. This base promoted (DIPEA) one-pot transformation i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867ac72de1f627bb05d6b0bcef4e5248
https://doi.org/10.1021/ol401336s
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6
Synthesis of Highly Functionalized 1,3-Oxathiazoles via an Unusual [4+1] Annulation alpha,alpha'-Dioxothione with 1,2-Diaza-1,3-dienes
Autor: Stefano Menichetti, Caterina Viglianisi, Orazio A. Attanasi, Gianfranco Favi, Fabio Mantellini, Giada Moscatelli
The present method provides highly functionalized 1,3-oxathioles through an unusual base-promoted [4+1] annulation between α,α'-dioxothione, generated in situ from a phthalimide precursor, and 1,2-diaza-1,3-dienes. An intriguing scaffold comprised
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a9562d26cb5398f801c6824059ce52
https://hdl.handle.net/11576/2579977
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7
ChemInform Abstract: A Novel Assembly of Substituted Pyrroles by Acid-Catalyzed Sequential Three-Component Reaction of Amines, Alkynoates, and 1,2-Diaza-1,3-dienes
Autor: Stefania Santeusanio, Orazio A. Attanasi, Fabio Mantellini, Gianfranco Favi, Giada Moscatelli
Publikováno v: ChemInform. 42
A novel protocol for the assembly of polysubstituted pyrroles has been developed through the acid-catalyzed, sequential three-component reaction of primary aliphatic amines, alkynoates and 1,2-diaza-1,3-dienes (DDs). This methodology proceeds with co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9443f5713efd9696061e3535445fc679
https://doi.org/10.1002/chin.201146103
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8
ChemInform Abstract: Synthesis of Functionalized Pyrroles via Catalyst- and Solvent-Free Sequential Three-Component Enamine-Azoene Annulation
Autor: Orazio A. Attanasi, Stefania Santeusanio, Fabio Mantellini, Giada Moscatelli, Gianfranco Favi
Publikováno v: ChemInform. 42
A new and efficient synthesis of polysubstituted pyrroles by a sequential one-pot three-component reaction between primary aliphatic amines, active methylene compounds, and 1,2-diaza-1,3-dienes (DDs) is reported. The reactions were performed without
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::14472d272e6abb10861fa3eee69f623c
https://doi.org/10.1002/chin.201130107
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9
Synthesis of functionalized pyrroles via catalyst- and solvent-free sequential three-component enamine-azoene annulation
Autor: Orazio A. Attanasi, Stefania Santeusanio, Gianfranco Favi, Fabio Mantellini, Giada Moscatelli
A new and efficient synthesis of polysubstituted pyrroles by a sequential one-pot three-component reaction between primary aliphatic amines, active methylene compounds, and 1,2-diaza-1,3-dienes (DDs) is reported. The reactions were performed without
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc6aad0cc89d88cc41f141c8d1a95977
https://hdl.handle.net/11576/2506753
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10
A novel assembly of substituted pyrroles by acid-catalyzed sequential three-component reaction of amines, alkynoates, and 1,2-diaza-1,3-dienes
Autor: Orazio A. Attanasi, Fabio Mantellini, Gianfranco Favi, Giada Moscatelli, Stefania Santeusanio
A novel protocol for the assembly of polysubstituted pyrroles has been developed through the acid-catalyzed, sequential three-component reaction of primary aliphatic amines, alkynoates and 1,2-diaza-1,3-dienes (DDs). This methodology proceeds with co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca2f42ca4f21c4ccf8c2cdf55f5ba78
https://hdl.handle.net/11576/2507149
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