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1
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85033134106
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PCT Int. Appl. WO 94 12,454
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Aoyama, H. PCT Int. Appl. WO 94 12,454; Chem. Abstr. 1994, 121, 179088b.
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(1994)
Chem. Abstr.
, vol.121
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Aoyama, H.1
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2
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85033145717
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note
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19F, δ -67.0 (d, J = 7.3 Hz).
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-
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3
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85033145557
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The Cu was a necessary ingredient for successful conversion of HCFC-123 to 1a-e
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The Cu was a necessary ingredient for successful conversion of HCFC-123 to 1a-e.
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4
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85033131611
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1a underwent hydrolysis in 10% HCl to give an 89% yield of the hydrate of trifluoroacetaldehyde
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1a underwent hydrolysis in 10% HCl to give an 89% yield of the hydrate of trifluoroacetaldehyde.
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6
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0000998149
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Gimbert, Y.; Moradpour, A.; Dive, G.; Dehareng, D.; Lahlil, K. J. Org. Chem. 1993, 58, 4685-4690.
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(1993)
J. Org. Chem.
, vol.58
, pp. 4685-4690
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Gimbert, Y.1
Moradpour, A.2
Dive, G.3
Dehareng, D.4
Lahlil, K.5
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8
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0000181842
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Fuchigami, T.; Yamamoto, K.; Nakagawa, Y. J. Org. Chem. 1991, 56, 137-142.
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(1991)
J. Org. Chem.
, vol.56
, pp. 137-142
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Fuchigami, T.1
Yamamoto, K.2
Nakagawa, Y.3
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9
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0000311134
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and references therein
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Crowley, P. J.; Percy, J. M.; Stansfield, K. Tetrahedron Lett. 1996, 37, 8233-8236, and references therein.
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(1996)
Tetrahedron Lett.
, vol.37
, pp. 8233-8236
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Crowley, P.J.1
Percy, J.M.2
Stansfield, K.3
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10
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0028846569
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Kodama, Y.; Yamane, H.; Okumura, M.; Shiro, M.; Taguchi, T. Tetrahedron 1995, 51, 12217-12228.
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(1995)
Tetrahedron
, vol.51
, pp. 12217-12228
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Kodama, Y.1
Yamane, H.2
Okumura, M.3
Shiro, M.4
Taguchi, T.5
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12
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85033154824
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note
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19F NMR: δ -114.1.
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13
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33947297094
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Fritsch, J. M.; Weingarten, H.; Wilson, J. D. J. Am. Chem. Soc. 1970, 92, 4038-4046.
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(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 4038-4046
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Fritsch, J.M.1
Weingarten, H.2
Wilson, J.D.3
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15
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0023736292
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Taguchi, T.; Kitagawa, O.; Suda, Y.; Ohkawa, S.; Hashimoto, A.; Iitaka, Y.; Kobayashi, Y. Tetrahedron Lett. 1988, 29, 5291-5294.
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(1988)
Tetrahedron Lett.
, vol.29
, pp. 5291-5294
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Taguchi, T.1
Kitagawa, O.2
Suda, Y.3
Ohkawa, S.4
Hashimoto, A.5
Iitaka, Y.6
Kobayashi, Y.7
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16
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0001458332
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Qian, C.-P.; Nakai, T.; Dixon, D. A.; Smart, B. E. J. Am. Chem. Soc. 1990, 112, 4602-4604.
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(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 4602-4604
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Qian, C.-P.1
Nakai, T.2
Dixon, D.A.3
Smart, B.E.4
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17
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0000028042
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Jin, F.; Jiang, B.; Xu, Y. Tetrahedron Lett. 1992, 33, 1221- 1224.
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(1992)
Tetrahedron Lett.
, vol.33
, pp. 1221-1224
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Jin, F.1
Jiang, B.2
Xu, Y.3
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18
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4344565765
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Yamana, M.; Ishihara, T.; Ando, T. Tetrahedron Lett. 1983, 24, 507-510.
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(1983)
Tetrahedron Lett.
, vol.24
, pp. 507-510
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Yamana, M.1
Ishihara, T.2
Ando, T.3
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19
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0030031231
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Kodama, Y.; Okumura, M.; Yanabu, N.; Taguchi, T. Tetrahedron Lett. 1996, 37, 1061-1064.
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(1996)
Tetrahedron Lett.
, vol.37
, pp. 1061-1064
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Kodama, Y.1
Okumura, M.2
Yanabu, N.3
Taguchi, T.4
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21
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0000907169
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Kitagawa, O.; Taguchi, T.; Kobayashi, Y. Tetrahedron Lett. 1988, 29, 1803-1806.
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(1988)
Tetrahedron Lett.
, vol.29
, pp. 1803-1806
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Kitagawa, O.1
Taguchi, T.2
Kobayashi, Y.3
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22
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1542609265
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Brigaud, T.; Doussoi, P.; Portella, C. J. Chem. Soc., Chem. Commun. 1995, 2117-2118.
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(1995)
J. Chem. Soc., Chem. Commun.
, pp. 2117-2118
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Brigaud, T.1
Doussoi, P.2
Portella, C.3
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23
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85033149784
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All given yields are based on 1a
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All given yields are based on 1a.
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24
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85033155755
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Products 7a-e and 8a-b were fully characterized by NMR, IR, HRMS, and CRN analysis
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Products 7a-e and 8a-b were fully characterized by NMR, IR, HRMS, and CRN analysis.
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-
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25
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85033152523
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The syntheses of 1a-e require an autoclave. Compound la is commercially available from SynQuest Laboratories, Inc., Alachua, FL
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The syntheses of 1a-e require an autoclave. Compound la is commercially available from SynQuest Laboratories, Inc., Alachua, FL.
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