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1
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33845279088
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Moss, R. A.; Wostowski, M.; Shen, S.; Krogh-Jespersen, K.; Matro, A. J. Am Chem. Soc. 1988, 110, 4443-4444.
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Moss, R.A.1
Wostowski, M.2
Shen, S.3
Krogh-Jespersen, K.4
Matro, A.5
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4
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0000609382
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and references cited therein
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Arduengo, A. J., III: Dias, H. V. R.; Dixon, D. A.; Harlow, R. L. Klooster, W. T., Koetzle, T. F. J. Am. Chem. Soc. 1994, 116, 6812-6822 and references cited therein.
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Arduengo III, A.J.1
Dias, H.V.R.2
Dixon, D.A.3
Harlow, R.L.4
Klooster, W.T.5
Koetzle, T.F.6
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10
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33847085566
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(f) Rondan, N. G.; Houk, K N., Moss, R. A. J. Am. Chem. Soc. 1980, 102, 1770-1776.
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Rondan, N.G.1
Houk, K.N.2
Moss, R.A.3
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11
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0002084580
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(g) Wong, T.; Warkentin, J., Terlouw, J. K. Int. J. Mass Spectrom. Ion Processes 1992, 115, 33-52.
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Int. J. Mass Spectrom. Ion Processes
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Wong, T.1
Warkentin, J.2
Terlouw, J.K.3
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12
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0000320226
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(a) El-Saidi, M.; Kassam, K., Pole, D. L.; Tadey, T., Warkentin, J. J. Am Chem Soc. 1992, 114, 8751-8752.
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El-Saidi, M.1
Kassam, K.2
Pole, D.L.3
Tadey, T.4
Warkentin, J.5
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13
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0000331336
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(b) Kassam, K.; Pole, D. L.; El-Saidi, M : Warkentin, J. J. Am. Chem Soc. 1994, 116, 1161-1162.
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Kassam, K.1
Pole, D.L.2
El-Saidi, M.3
Warkentin, J.4
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14
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15844364059
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Ph.D. Thesis. McMaster University. Hamilton. Ontario. Canada
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Compound 7a was previously prepared by a similar method: Zoghbi. M. Ph.D. Thesis. McMaster University. Hamilton. Ontario. Canada, 1991.
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(1991)
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Zoghbi, M.1
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15
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15844362893
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note
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The identity of oxadiazolines 7b.d-g was confirmed by mass spectrometric experiments involving LRP and HRP electron impact, colisional activation spectrometry. and chemical ionization using ammonia. Results are available as supporting information.
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18
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15844417776
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note
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-4 mol of oxadiazoline in 10 mL of benzene.
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-
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22
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15844385135
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note
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3).
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24
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0001836924
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Sonoda, N.; Yamamoto, G.; Natsukawa, K.; Kondo, K.; Murai, S. Tetrahedron Lett. 1975, 1969-1972.
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(1975)
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, pp. 1969-1972
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Sonoda, N.1
Yamamoto, G.2
Natsukawa, K.3
Kondo, K.4
Murai, S.5
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26
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0011694851
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Fujiwara, M.; Baba, A.; Matsuda, H. J. Heterocycl. Chem. 1989, 26, 1659-1663.
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(1989)
J. Heterocycl. Chem.
, vol.26
, pp. 1659-1663
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Fujiwara, M.1
Baba, A.2
Matsuda, H.3
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27
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15844414741
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note
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The concentration of 10f was too low to allow its measurement by integration of the NMR signals: however. 10f was isolated from a larger scale thermolysis in ca. 2% yield.
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28
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0348055770
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Shibata, I.; Nakamura, K.; Baba. A.; Matsuda. H. Bull. Chem. Soc. Jpn. 1989, 62, 853-859.
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(1989)
Bull. Chem. Soc. Jpn.
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, pp. 853-859
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Shibata, I.1
Nakamura, K.2
Baba, A.3
Matsuda, H.4
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29
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84982074567
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Hoffmann, R. W.; Lilienblum, W.; Dittrich, B. Chem. Ber. 1974, 107, 3395-3407.
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(1974)
Chem. Ber.
, vol.107
, pp. 3395-3407
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Hoffmann, R.W.1
Lilienblum, W.2
Dittrich, B.3
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31
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15844399188
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Two diastereomers are possible
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Two diastereomers are possible.
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