## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Synthesis of Azapyrrolo[3,2,1-jk]carbazoles, Azaindolo[3,2,1-jk]carbazoles, and Carbazole-1-carbonitriles by Gas-Phase Cyclization of Aryl Radicals
β Scribed by Crawford, Lynne; McNab, Hamish; Mount, Andrew; Verhille, Jeanne; Wharton, Stuart
- Book ID
- 121528300
- Publisher
- Thieme Medical Publishers
- Year
- 2010
- Tongue
- German
- Weight
- 122 KB
- Volume
- 2010
- Category
- Article
- ISSN
- 0039-7881
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π SIMILAR VOLUMES
## Abstract Pyrido[3,2,1β__jk__]carbazoles **1**, synthesized from carbazoles and alkylβ or arylmalonates, gave regioselective electrophilic substitution reactions at position 5 such as chlorination to 5βchloro derivatives **2**, nitration to 5βnitro compounds **3**, or hydroxylation to 5βhydroxy d
4-Hydroxy-5-phenylpyrido[3,2,1-jk]carbazol-6-ones (4, 5), which were obtained from carbazoles 1 and malonates 2 or 3, were converted to reactive intermediates such as 4-chlorides 9 or 4-tosylates 10, which gave in turn 4-azido-5-phenyl derivatives 11. 5-Alkyl-4-azides 11 were not obtained in this ma