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The synthesis of novel polycyclic heterocyclic ring systems via photocyclization. 22 Dibenzo[f,h]benzothieno[2,3-c]quinoline, dibenzo[f,h]benzothieno[2,3-c][1,2,4]triazolo[4,3-a]quinoline and dibenzo[f,h]naphtho[2′,1′:4,5]thieno[2,3-c]quinoline

✍ Scribed by Jiann-Kuan Luo; Maria P. Cabal; Ronald F. Federspiel; Raymond N. Castle


Publisher
Journal of Heterocyclic Chemistry
Year
2000
Tongue
English
Weight
325 KB
Volume
37
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

Photocyclization of 3‐chloro‐N‐(9‐phenanthryl)benzo[b]‐thiophene‐2‐carboxamide (3) and 3‐chloro‐N‐(9‐phenanthryl)‐naphtho[1,2‐b]thiophene‐2‐carboxamide (10) yielded dibenzo[f,h]benzothieno[2,3‐c]‐quinolin‐10(9__H__)‐one (4) and dibenzo[f,h]naphtho[2′,1′:4,5]thieno[2,3‐c]quinolin‐10(9__H__)‐one (11), respectively. Further elaboration of the lactams provided three novel unsubstituted new ring systems.


📜 SIMILAR VOLUMES


The synthesis of novel polycyclic hetero
✍ Jiann-Kuan Luo; Ronald F. Federspiel; Raymond N. Castle 📂 Article 📅 1997 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 351 KB 👁 1 views

## 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

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✍ Jiann-Kuan Luo; Ronald F. Federspiel; Raymond N. Castle 📂 Article 📅 1998 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 347 KB

## Abstract Four previously unknown polycyclic heterocyclic ring systems, namely, benzo[__h__]thieno[3′,2′:4,5]‐thieno[2,3‐__c__]quinoline (6), benzo[__h__]thieno[3′,2′:4,5]thieno[2,3‐__c__]quinoline (11), benzo[__f__]thieno‐[3′,2′:4,5]thieno[2,3‐__c__]tetrazolo[1,5‐__a__]quinoline (12) and benzo[_

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## 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

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