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Chemistry of propadiene. II. The addition of dichlorocarbene to propadiene

✍ Scribed by H. G. Peer; A. Schors


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
287 KB
Volume
86
Category
Article
ISSN
0165-0513

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πŸ“œ SIMILAR VOLUMES


The chemistry of propadiene: Some invest
✍ H. G. Peer πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 491 KB

## Abstract The reaction of propadiene with Br~2~, BrCl, and Cl~2~ is studied in various solvents and at different temperatures. It is shown that only partial addition takes place, and further that the initial attack of the Hal^+^ ion takes place at the central C atom. The findings are interpreted

Sigmatropic Rearrangements Accompanying
✍ Charles W. Jefford; GΓ©rald Bernardinelli; Jean-Claude Rossier; Jacques A. Zuber πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 German βš– 160 KB

## Abstract A new product arising from the reaction of dichlorocarbene with norbornadiene, 6__endo__‐(2,2‐dichlorovinyl)‐__cis__‐bicyclo[3.1.0]hex‐2‐ene, is described. It does not arise from the normal __exo__‐l,2‐adduct, but possibly originates by sigmatropic rearrangement of an initially formed z

Steric hindrance in the addition of dich
✍ Robert A. Moss; Andrew Mamantov πŸ“‚ Article πŸ“… 1968 πŸ› Elsevier Science 🌐 French βš– 177 KB

A recent reactivity comparison of dichlorocarbene and chlorofluorocarbene suggested that steric hindrance played an important role in determining the rate of the carbene-olefin addition reaction (1). Indeed, although warnings were is-