Paper
Bicyclo[2.2.0]hex-1(4)-ene.
Published 1986 · K. B. Wiberg, M. G. Matturro, P. Okarma
Tetrahedron
Q3 SJR score
47
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Bicyclo[2.2.0]hex-1(4)-ene is a highly reactive alkene with potential applications in preparing [m.2.2]propellanes through dimerization and cycloaddition reactions.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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Citations
Building up Strain in One Step: Synthesis of an Edge‐Fused Double Silacyclobutene from an Extensively Trichlorosilylated Butadiene Dianion
This study demonstrates a one-step synthesis of an edge-fused double silacyclobutene from an exhaustively trichlorosilylated butadiene dianion, resulting in a stable, C=C double-bonded compound with high stability up to 180°C.
2020·2citations·Isabelle Georg et al.·Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International Ed. in English)
Chemistry of the Highly Strained Alkene Perfluorobicyclo[2.2.0]hex‐1(4)‐ene
This study reveals the chemistry of the highly strained alkene perfluorobicyclo[2.2.0]hex1(4)ene, leading to the discovery of rare [2.2.2]propellane ring systems and their transformations through quantum mechanical calculations.
2018·2citations·C. Junk et al.·European Journal of Organic Chemistry
European Journal of Organic Chemistry
Competitive 1,2-C Atom Shifts in the Strained Carbene Spiro[3.3]hept-1-ylidene Explained by Distinct Ring-Puckered Conformers.
Spiro[3.3]hept-1-ylidene undergoes two 1,2-sigmatropic rearrangements, with ring-contraction yielding cyclopropylidenecyclobutane and ring-expansion yielding bicyclo[3.2.0]hept-1(5)-en
2016·12citations·M. G. Rosenberg et al.·The Journal of organic chemistry
The Journal of organic chemistry
Tracing the Fingerprint of Chemical Bonds within the Electron Densities of Hydrocarbons: A Comparative Analysis of the Optimized and the Promolecule Densities.
The study reveals a unified mode of density accumulation for C-H bonds, but various modes for C-C bonds, revealing four distinct groups.
2016·12citations·Z. Keyvani et al.·Chemphyschem : a European journal of chemical physics and physical chemistry
Chemphyschem : a European journal of chemical physics and physical chemistry
Synthesis and properties of the strained alkene perfluorobicyclo[2.2.0]hex-1(4)-ene.
The strained alkene perfluorobicyclo[2.2.0]hex-1(4)-ene is a stable, highly reactive fluoroalkene with high yield and purity.
2015·5citations·C. Junk et al.·The Journal of organic chemistry
The Journal of organic chemistry