## Abstract Photocyclization of 3‐chloro‐__N__‐(3‐phenanthryl)naphtho[1,2‐__b__]thiophene‐2‐carboxamide (**12**) furnished only one of the two possible isomers, __i.e.__, naphtho[2′,1′:4,5]thieno[2,3‐__c__]naphtho[1,2‐__f__]quinolin‐6(5__H__)‐one (**13**), which was further elaborated to yield the
1,2-dihydro-1,2,4,3-triazaphospholo[4,5-a]quinolines as electron carriers in the electrochemical reduction of 1,1-dichloro-2-methoxycarbonyl-2-methylcyclopropane
✍ Scribed by V. V. Yanilkin; B. I. Buzykin; R. M. Eliseenkova; N. I. Maksimyuk; N. V. Nastapova
- Publisher
- Springer
- Year
- 1999
- Tongue
- English
- Weight
- 257 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1573-9171
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## 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 “Full Text” option. The original article is trackable v
## Abstract Photocyclization of 3‐chloro‐N‐(3‐phenanthryl)thieno[2,3‐__b__]thiophene‐2‐carboxamide (5) yielded only one of the two possible structural isomers, thieno[3′,2′:4,5]thieno[2,3‐__c__]naphtho[1,2‐__f__]quinolin‐6(5__H__)‐one (6), which was further elaborated to afford the unsubstituted ri
## Abstract For Abstract see ChemInform Abstract in Full Text.