-
1
-
-
60949101645
-
-
Boonlarppradab, C.; Kauffman, C. A.; Jensen, P. R.; Fenical, W. Org. Lett. 2008, 10, 5505-5508.
-
(2008)
Org. Lett.
, vol.10
, pp. 5505-5508
-
-
Boonlarppradab, C.1
Kauffman, C.A.2
Jensen, P.R.3
Fenical, W.4
-
3
-
-
37649016653
-
-
(b) Williamson, N. R.; Fineran, P. C.; Gristwood, T.; Chawrai, S. R.; Leeper, F. J.; Salmond, G. P. C. Future Microbiol. 2007, 2, 605-618.
-
(2007)
Future Microbiol.
, vol.2
, pp. 605-618
-
-
Williamson, N.R.1
Fineran, P.C.2
Gristwood, T.3
Chawrai, S.R.4
Leeper, F.J.5
Salmond, G.P.C.6
-
4
-
-
77749273799
-
-
Aldrich, L. N.; Dawson, E. W.; Lindsley, C. W. Org. Lett. 2010, 12, 1048-1051.
-
(2010)
Org. Lett.
, vol.12
, pp. 1048-1051
-
-
Aldrich, L.N.1
Dawson, E.W.2
Lindsley, C.W.3
-
5
-
-
0034872156
-
-
(a) Cerdenõ, A. M.; Bibb, M. J.; Challis, G. L. Chem. Biol. 2001, 8, 817-829.
-
(2001)
Chem. Biol.
, vol.8
, pp. 817-829
-
-
Cerdenõ, A.M.1
Bibb, M.J.2
Challis, G.L.3
-
6
-
-
33751102631
-
-
(b) Williamson, N. R.; Fineran, P. C.; Leeper, F. J.; Salmond, G. P. C. Nat. Rev. Microbiol, 2006, 4, 887-899.
-
(2006)
Nat. Rev. Microbiol
, vol.4
, pp. 887-899
-
-
Williamson, N.R.1
Fineran, P.C.2
Leeper, F.J.3
Salmond, G.P.C.4
-
7
-
-
39149120828
-
-
(c) Mo, S.; Sydor, P. K.; Corre, C.; Alhamadsheh, M. M.; Stanley, A. E.; Haynes, S. W.; Song, L.; Reynolds, K. A.; Challis, G. L. Chem. Biol. 2008, 15, 137-148.
-
(2008)
Chem. Biol.
, vol.15
, pp. 137-148
-
-
Mo, S.1
Sydor, P.K.2
Corre, C.3
Alhamadsheh, M.M.4
Stanley, A.E.5
Haynes, S.W.6
Song, L.7
Reynolds, K.A.8
Challis, G.L.9
-
8
-
-
0041366893
-
-
Hydrogenolysis of a keto isoxaoline afforded a compound whose spectral data are in agreement with those of a hemi-iminal. See compound 12 in: Andersen, S. H.; Sharma, K. K.; Torssell, K. B. G. Tetrahedron 1983, 39, 2241-2245.
-
(1983)
Tetrahedron
, vol.39
, pp. 2241-2245
-
-
Andersen, S.H.1
Sharma, K.K.2
Torssell, K.B.G.3
-
9
-
-
0016234042
-
-
Cohen, N.; Banner, B. L.; Blount, J. F.; Weber, G.; Tsai, M.; Saucy, G. Org. Chem. 1974, 39, 1824-1833.
-
(1974)
Org. Chem.
, vol.39
, pp. 1824-1833
-
-
Cohen, N.1
Banner, B.L.2
Blount, J.F.3
Weber, G.4
Tsai, M.5
Saucy, G.6
-
10
-
-
0004419437
-
-
Cycloadditions with the nitrile N-oxide derived from benzaldehyde oxime can be carried out at room temperature, whereas diose with the nitrile N-oxide derived from the oxime of pyrrole-2-carboxaldehyde must be carried out at -70 °C See: Ghabrial, S. S.; Thomsen, I.; Torssell, K. B. G. Acta chem. Scand. B 1987, B41, 426-434.
-
(1987)
Acta Chem. Scand. B
, vol.B41
, pp. 426-434
-
-
Ghabrial, S.S.1
Thomsen, I.2
Torssell, K.B.G.3
-
11
-
-
26844495248
-
-
For a similar effect by an axial oxygen in spiroketals, see: Doubský, J.; Saman, D.; Zedník, J.; Vašíč ková, S.; Koutek, B. Tetrahedron Lett. 2005, 46, 7923-7926.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 7923-7926
-
-
Doubský, J.1
Saman, D.2
Zedník, J.3
Vašíč ková, S.4
Koutek, B.5
-
12
-
-
33751091528
-
-
Jolicoeur, B.; Chapman, E. E.; Thompson, A.; Lubell, W. D. Tetrahedron 2006, 62, 11531-11563.
-
(2006)
Tetrahedron
, vol.62
, pp. 11531-11563
-
-
Jolicoeur, B.1
Chapman, E.E.2
Thompson, A.3
Lubell, W.D.4
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