## Abstract The sulfonation of isopyrene (1) and its 5‐methyl‐ and 5,10‐dimethyl derivative 2 and 3 with SO~3~ in both dichloromethane and nitromethane as solvent has been studied. Reaction of 1 and 2 leads to sulfodehydrogenation in which SO~3~ reacts as a monodentate electrophile, the initial pro
On the relative reactivity of the C C double bond and the [10] annulene moiety versus SO3
✍ Scribed by Hans J. A. Lambrechts; Hans Cerfontain
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 153 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Sulfonation of 11‐methylene‐1,6‐methano[10]annulene (6a) with 1, 3, 4 or 6 equivalents of the dioxane‐SO~3~ complex in dioxane results in the formation of the 2‐sulfonic acid (6b) as the exclusive ^1^H NMR detectable product, whereas 1,6‐methano‐[10]annulene (5a) with 3 equiv. of this sulfonating agent already yields the 2,7‐disulfonic acid. The lower reactivity of the peripheral ring of 6a compared with that of 5a is explained in terms of a higher coplanarity of the annulene ring of 6a.
📜 SIMILAR VOLUMES
The reactivity of the -C(Cl)@C-C@N-moiety towards an AlCl 3 -induced C-C bond forming reaction was investigated through the reaction of 7-chloro-5-phenyl-pyrazolo[1,5-a]pyrimidine with arenes and heteroarenes. This study furnished a novel and highly selective methodology for the preparation of 7-(he
## Abstract 2D NOESY, COSY and ^31^P,^1^H correlation measurements have been carried out on the optically active β‐pineneallyl‐(__R__)(+)‐BINAP palladium complex, [Pd(η^3^‐C~10~H~15~){(__R__)(+)‐BINAP}](CF~3~SO~3~). The __ortho__ protons of the four non‐equivalent phenyl rings have been assigned, a