對1-疊氮

Flash vacuum pyrolysis (FVP) of 1-azidoindene, which via a nitrene intermediate, gave some products of rearrangement：quinoline、isoquinoline and 1-methylene-1H-isoindole。Under pyrolytic conditions, 3-(4-methoxystyryl)thiophene could get a radical intermediate and gave 3-(4-hydroxystyryl)thiophene, or it gave contractive tricyclic compounds which having signals on spectrum but inseparable, like as indene structures.

目錄


第一章 1-疊氮

第一章
1.Tiemann, F. Chem. Ber. 1891, 24, 4162-4166.
2.Lwowski, W. Nitrenes, John Wiley and Sons, Inc.: New York, 1970.
3.Wentrup, C. Reactive Molecules, John Wiley and Sons, Inc.: New York, 1984; pp, 162-264.
4.Folwer, F. W.; Hassner, A.; Levy, LA. J. Am. Chem. Soc. 1967, 89, 2077-2082.
5.Platz, M. S.; Carrol, G.; Pierrat, E.; Zayas, J.; Auster, S. Tetrahedron 1982, 38, 777-785.
6.Crow, W. D.; Wentrup, C. Tetrahedron Lett. 1967, 4379-4384.
7.Swenton, J. S. Tetrahedron Lett. 1967, 2855-2857.
8.Wentrup, C. Tetrahedron Lett. 1971, 27, 1027-1030.
9.Splitter, J. S.; Calvin, M. Tetrahedron Lett. 1968, 1445-1448.
10.Lwowski, W.; Maricich, T. J. J. Am. Chem. Soc. 1965, 87, 3630-3637.
11.Sunndberg, R. J. Am. Chem. Soc. 1966, 88, 3781-3789.
12.(a) Atkinson, R. S., Judkins, B. D.; Khan, N. J. Chem. Soc. Perkin Trans. I 1982, 2491-2497; (b) Atkinson, R. S., Judkins, B. D.; Khan, N. J. Chem. Soc. Perkin Trans. I 1981, 2615-2619.
13.Crow, W. D.; Wentrup, C. Tetrahedron Lett. 1968, 6149-6152.
14.Wentrup, C. Chem. Commun. 1969, 1386-1387.
15.Wentrup, C. Chem. Commun. 1969, 1386-1387.
16.Sumitani, M.; Nagakura, S.; Yoshihara, K. Bull. Chem. Soc. Jpn. 1976, 49, 2995-2998.
17.Lwowski, W. Angew. Int. Ed. Engl. 1967, 6, 897-906.
18.Nicholas, P. P. J. Org. Chem. 1975, 40, 3396-3398.
19.Smolinsky, G.; Feuer, B. I. J. Org. Chem. 1966, 31, 3882-3884.
20.Moriarty, R. M.; Rahman, M. Tetrahedron 1965, 21, 2877-2891.
21.Abramovitch, R. A.; Kyba, E. P. Chem. Common. 1969, 265-266.
22.Wentrup, C. Adv. Heterocycl. Chem. 1981, 28, 231-361.
23.Wentrup, C.; Winter, H. W. J. Am. Chem. Soc. 1980, 102, 6159-6161.
24.Crow. W. D.; Wentrup, C. Chem. Commun. 1969, 1386-1387.
25.國立中山大學研究所研究生邱紹榕之博士論文，中華民國八十九年六月。
26.國立中山大學研究所研究生陳秉樞之博士論文，中華民國八十六年六月。
27.國立中山大學研究所研究生朱立澤之碩士論文，中華民國八十八年六月。
28.國立中山大學研究所研究生廖士傑之碩士論文，中華民國八十二年六月。
29.國立中山大學研究所研究生楊維智之碩士論文，中華民國八十五年六月
30.國立中山大學研究所研究生朱健誠之碩士論文，中華民國八十八年六月。
31.國立中山大學研究所研究生林宗德之碩士論文，中華民國九十年六月。
32.國立中山大學研究所研究生許躍騰之93年化學年會公開發表論文壁報。
33.Banert, K.; Hagedorn, M.; Liedtke, C.; Melzer, A. Eur. J. Org. Chem. 2000, 257-267.
34.Murphy, J. A.; Patterson, C. W. J. Chem. Soc. Perkin Trans. 1 1993, 405-410.
35.James, B.; Philip, B. J. Org. Chem. 1980, 45, 5213.
36.Billimoria, J. D.; Maclagen, N. F. J. Chem. Soc. 1954, 3257-3262.
37.Ibrahim, Y. A.; Al-Awadi, N. A.; Kual, K. Tetrahedron 2003, 59, 5425-5430.
38.Ferri, D.; Bűrgi, T. J. Am. Chem. Soc. 2001, 123, 12074-12084.
39.Crisp, G. T.; Papadopoulos, S. Aust. J. Chem. 1989, 42, 279-285.
40.Wehrli, P. A.; Schaer, B. Synthesis 1974, 288-289.

第二章
1. Hammond, G. S.; Saltiel, J. J. Am. Chem. Soc. 1962, 84, 4983-4984.
2. Mallory, F. B.; Wood, C. S.; Gordon, J. T.; Lindquist, L. C.; Savitz, M. L. J. Am. Chem. Soc. 1962, 84, 4361-4362.
3. Kupchan, S. M.; Wormser, H. C. Tetrahedron Lett. 1965, 6, 359-363.
4. Lewis, F. D. Acc. Chem. Res. 1979, 12, 152-158.
5. (a) Lewis, F. D.; Ho. T.-I.; Simpson, J. T. J. Am. Chem. Soc. 1982, 104, 1924-1929. (b) Yasuda, M.; Isami, T.; Kubo, J.; Mizutani, M.; Yamashita, T.; Shima, K. J. Org. Chem. 1992, 57, 1351-1354. (c) Lewis, F. D.; Ho, T.-I.; Simpson, J. T. J. Org. Chem. 1981, 46, 1077-1082.
6. Somers, J. B. M.; Couture, A.; Lablache-Combier, A.; Laarhoven, W. H. J. Am. Chem. Soc. 1985, 107, 1387-1394.
7. Mallory, F. B.; Wood, C. S.; Gordon, J. T. J. Am. Chem. Soc. 1964, 86, 3094-3102.
8. Curruthers, W.; Stewart, H. N. W. Tetrahedron Lett. 1965, 6, 301-302.
9. Loader, C. E.; Timmons, C. J. J. Chem. Soc. (C) 1967, 1677-1681.
10. Ho, T. I.; Wang, S. Li.; Wu, J. Y. Angew. Chem. Int. Ed. 1999, 38, 2558-2560.
11. Turro, N. J.; Ramamurthy, V.; Cerry, W.; Farneth, W. Chem. Rev. 1978, 78, 125-145.
12. Saito, M.; Kamei, Y.; Kuribara, K.; Yoshioka, M. J. Org. Chem. 1998, 63, 9013-9018.
13. Huyser, E. S.; Neckers, D. C. J. Org. Chem. 1964, 29, 276-278.
14. (a) Ho, T. I.; Ho, J. H.; Wu, J. Y. J. Am. Chem. Soc. 2000, 122, 8575-8576. (b) Ho, J. H.; Ho, T. I.; Liu, R. S. H. Org. Lett. 2001, 3, 409-411.
15. Ho, J. H.; Ho, T. I. Tetrahedron Lett. 2003, 44, 4669-4672.
16. Plater, M. J. Tetrahedron Lett. 1994, 35, 801-802.
17. 國立中山大學研究所研究生朱立澤之博士論文，中華民國九十四年六月。
18. Harrison, A. G.; Honnen, L. R.; Dauben, Jr., H. J.; Lossing, F. P. J. Am. Chem. Soc. 1960, 82, 5593-5598.
19. Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95-109.