1.trans o-methoxystilbene and its derivatives 47a-f had been studied by means of pyrolysis and photolysis. Under pyrolytic conditions, compounds 47a-f gave not only the expected products 52a,c-f, but also their corresponding isomers 53a,c-f . Furthermore, compound 47b gave naphthalene (63) as the major product by opening the furan ring at higher temperature. Under photolytic conditions, compounds 47a-f gave the expected photocyclic products 2a-f and 109a-f.2.Pyrolytic chemistry of N-(N-Methyl-3-indolyl)methyl benzamide (45) hes been studied. Pyrolysis of 45 gave 3-methyl quinoline (38), 4-methyl quinoline (39) and secondary pyrolysis product quinoline (36).
2.Pyrolytic chemistry of N-(N-Methyl-3-indolyl)methyl benzamide (45) hes been studied. Pyrolysis of 45 gave 3-methyl quinoline (38), 4-methyl quinoline (39) and secondary pyrolysis product quinoline (36).
| Identifer | oai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0727109-191937 |
| Date | 27 July 2009 |
| Creators | Syu, Jhih-Peng |
| Contributors | Teng-Yuan Dong, Chin-Hsing Chou, Eng-Chi Wang |
| Publisher | NSYSU |
| Source Sets | NSYSU Electronic Thesis and Dissertation Archive |
| Language | Cholon |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0727109-191937 |
| Rights | not_available, Copyright information available at source archive |
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