Cyclooctatetraene ohne Bindungsaustausch
β Scribed by Prof. Dr. D. Bryce-Smith; Dr. A. Gilbert; J. Grzonka
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- English
- Weight
- 236 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Only two examples of cycloaddition to ynamines have so far been reported 121. By 1,3-dipolar cycloaddition under the conditions described previously 131, ynamines readily afford dialkylamino-substituted heterocycles ( I ) (Table 1). The structure of the products follows from analytical data and in a
Ial Compound (61. tbl Compound (5). carboxylation with lead tetraacetate in the presence of pyridine [21. Hydroxylation of (2) with performic acid gave a mixture of glycols, consisting mainly of cis-1,2,3,4-dibenzocis-configuration of this glycol was shown by its identity with the compound obtained
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