Results 111 to 120 of about 1,453 (161)
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Isomerisation of Vinyl Sulfones for the Stereoselective Synthesis of Vinyl Azides
European Journal of Organic Chemistry, 2020Reported is the construction, and facile base‐mediated conversation of ten differently substituted 3‐azido E‐vinyl sulfones (γ‐azido‐α,β‐unsaturated sulfones) into their isomeric vinyl azide counterparts. The requisite 3‐azido E‐vinyl sulfones were prepared from 3‐bromo E‐vinyl sulfones, which in turn were accessed from allyl sulfones via a bromination‐
Collins, Niall +3 more
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Canadian Journal of Chemistry, 1973
Reaction of vinyl azides with nitrosyl tetrafluoroborate yields 1,2,5-oxadiazoles and 1,2,4-oxadiazoles depending on the structure of the azide. Reaction of 1,2-dialkyl vinyl azides with nitryl tetrafluoroborate gives 2-oxo-1,2,5-oxadiazoles in high yields whereas 1-aryl-2-alkyl vinyl azides gave moderate yields of 3-aryl-1,2,5-oxadiazoles and 5-aryl ...
A. N. Thakore +2 more
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Reaction of vinyl azides with nitrosyl tetrafluoroborate yields 1,2,5-oxadiazoles and 1,2,4-oxadiazoles depending on the structure of the azide. Reaction of 1,2-dialkyl vinyl azides with nitryl tetrafluoroborate gives 2-oxo-1,2,5-oxadiazoles in high yields whereas 1-aryl-2-alkyl vinyl azides gave moderate yields of 3-aryl-1,2,5-oxadiazoles and 5-aryl ...
A. N. Thakore +2 more
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Computational Study on the Vinyl Azide Decomposition
The Journal of Physical Chemistry A, 2014The decomposition mechanism of vinyl azide (CH2CHN3) has been studied by calculations of the electronic structure. In addition, a study based on the topology of the electron charge density distribution and its Laplacian function, within the Quantum Theory of Atoms in Molecules (QTAIM), has been carried out with the aim of comprehending the electron ...
Darío J R, Duarte +2 more
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Tetrahedron Letters, 1979
Abstract Vinyl cations generated by the title photolysis gave vinyl azides by capture of an azide ion and their further photolyses resulted in the formation of cycloaddition-products via nitrile ylides derived from the corresponding azirines.
Tsugio Kitamura +2 more
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Abstract Vinyl cations generated by the title photolysis gave vinyl azides by capture of an azide ion and their further photolyses resulted in the formation of cycloaddition-products via nitrile ylides derived from the corresponding azirines.
Tsugio Kitamura +2 more
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Reactions of Fluoroalkanesulfonyl Azides with Cyclic Vinyl Ethers.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Shi-Zheng Zhu +2 more
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Chemischer Informationsdienst, 1979
AbstractAus dem Vinylbromid (I) erhält man bei der Photolyse in Gegenwart von Tetrabutylammoniumazid (II) über diskutierte Zwischenstufen das Folgeprodukt (III).
T. KITAMURA, S. KOBAYASHI, H. TANIGUCHI
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AbstractAus dem Vinylbromid (I) erhält man bei der Photolyse in Gegenwart von Tetrabutylammoniumazid (II) über diskutierte Zwischenstufen das Folgeprodukt (III).
T. KITAMURA, S. KOBAYASHI, H. TANIGUCHI
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ChemInform Abstract: VINYL AZIDES AS DIAZOENAMINES
Chemischer Informationsdienst, 1973AbstractIn Abhängigkeit von der Struktur reagieren Vinylazide mit NOBF4 zu l,2,5‐ und 1,2,4‐Oxadiazolen.
A. N. THAKORE +2 more
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The microwave spectrum of vinyl azide
Journal of Molecular Spectroscopy, 1977Abstract Vinyl azide has been shown to exist in both cis and trans conformations with the cis more stable by 460 cal/mole. The rotational constants in Megahertz are: cis, A = 14 698.23, B = 4088.44, C = 3195.64; trans, A = 46 761.19, B = 2751.40, C = 2598.83.
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Fluorocyclization of Vinyl Azides for the Formation of 3‐Azido Heterocycles
Chemistry – An Asian Journal, 2020Abstract3‐Azido saturated heterocycles are important for therapeutic‐development but challenging to prepare. Disclosed herein is a novel synthetic strategy for 3‐azido heterocycles via fluorocyclization of the easily available vinyl azides. This transfor‐mation proceeded under mild conditions and provided a wide range of 3‐azido heterocycles in good to
Diangang Bai +6 more
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Thermal and photochemical annulation of vinyl azides to 2-aminoimidazoles
Organic & Biomolecular Chemistry, 2019The rapid and facile generation of diverse 2-aminoimidazoles via thermal or photochemical activation of vinyl azides has been investigated.
Lucas Man +2 more
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