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Benzylation of 1‐Benzylidene‐3‐Pyrazolidinium Oxides

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TLDR
The benzylation of 1-benzylidene-5-phenyl-3-pyrazolidinium oxide (2a) gives five products including the head-to-head dimer of 2 (7) and the ring-opened 1-(1)-cinnamoylbenzalhydrazone (4a) as discussed by the authors.
Abstract
The benzylation of 1-benzylidene-5-phenyl-3-pyrazolidinium oxide (2a) gives five products including the “head to head” dimer of 2 (7) and the ring-opened 1-benzyl-1-cinnamoylbenzalhydrazone (4a). Similar behavior was also observed with ylides bearing various substituents at the 4 and 5 positions.

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Cyclization and cycloaddition of 1-cinnamylidene-5-phenyl-3-oxopyrazolidinium ylide

TL;DR: In this article, a cycloaddition of 1-cinnamylidene-5-phenyl-3-oxopyrazolidinium ylide (1b) to the anticipated bicyclic [3.3.0] pyrazolidine is presented.
Journal ArticleDOI

Diphenylacetylene from the Base‐Catalyzed Fragmentation of 3,6‐Dihydro‐5,6‐Diphenyl‐3‐Tosyl‐1,3,4‐Oxadiazin‐2‐One

TL;DR: Treatment of 3,6-dihydro-5, 6-diphenyl-3-tosyl-1,3,4-oxadiazin-2-one with sodium hydride in THF affords diphenylacetylene in better than 70% yield as discussed by the authors.
Journal ArticleDOI

Benzylation of 1-Benzylidene-3-pyrazolidinium Oxides.

TL;DR: The benzylation of 1-benzylidene-5-phenyl-3-pyrazolidinium oxide (2a) gives five products including the head-to-head dimer of 2 (7) and the ring-opened 1-(1)-cinnamoylbenzalhydrazone (4a) as mentioned in this paper.
References
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Journal ArticleDOI

Chemistry of Aminimides

Stanley Wawzonek
- 01 Jun 1973 - 
Journal ArticleDOI

Die Chemie der Amin‐N‐imine

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Addition-addition-elimination mechanism of 1,3-dipole “dimerization”

Helmut Dorn, +1 more
- 01 Jan 1988 - 
TL;DR: In this paper, the three-step ADD-ADD-EL pathway to thermal "dimers" of pyrazolidin-3-one-azomethinimines without a center of symmetry is presented.
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