-
1
-
-
0028198228
-
-
Perry N.B., Ettouati L., Litaudon M., Blunt J.W., Munro M.H.G., Parkin S., Hope H. Tetrahedron. 50:1994;3987-3992.
-
(1994)
Tetrahedron
, vol.50
, pp. 3987-3992
-
-
Perry, N.B.1
Ettouati, L.2
Litaudon, M.3
Blunt, J.W.4
Munro, M.H.G.5
Parkin, S.6
Hope, H.7
-
2
-
-
0028230338
-
-
Trimurtulu G., Faulkner D.J., Perry N.B., Ettouati L., Litaudon M., Blunt J.W., Munro M.H.G., Jameson G.B. Tetrahedron. 50:1994;3993-4000.
-
(1994)
Tetrahedron
, vol.50
, pp. 3993-4000
-
-
Trimurtulu, G.1
Faulkner, D.J.2
Perry, N.B.3
Ettouati, L.4
Litaudon, M.5
Blunt, J.W.6
Munro, M.H.G.7
Jameson, G.B.8
-
11
-
-
85031142184
-
-
13C NMR, MS and HRMS spectra were consistent for all new compounds.
-
13C NMR, MS and HRMS spectra were consistent for all new compounds.
-
-
-
-
14
-
-
85031143305
-
-
3, 75 MHz) 18.6, 19.3 (t); 21.6 (q); 25.2, 25.3 (t); 30.0, 30.2 (d); 43.3 and 44.9 (t); 55.6 (q); 61.9 and 62.3 (t); 62.7 and 63.5 (d); 95.5 and 96.4 (d); 101.3 and 101.4 (d); 102.9 (d); 111.9 (s); 126.2 (s); 126.4 (d); 129.2 (d); 129.3 (s); 132.2 (s); 142.5 (s); 147.6 and 150.0 (d); 159.7 (s).
-
3, 75 MHz) 18.6, 19.3 (t); 21.6 (q); 25.2, 25.3 (t); 30.0, 30.2 (d); 43.3 and 44.9 (t); 55.6 (q); 61.9 and 62.3 (t); 62.7 and 63.5 (d); 95.5 and 96.4 (d); 101.3 and 101.4 (d); 102.9 (d); 111.9 (s); 126.2 (s); 126.4 (d); 129.2 (d); 129.3 (s); 132.2 (s); 142.5 (s); 147.6 and 150.0 (d); 159.7 (s).
-
-
-
-
15
-
-
85031138229
-
-
6, 75 MHz): 21.0 (q); 55.9 (q); 93.0 (d); 102.1 (d); 113.9 (s); 120.2 (d); 124.4 (d); 125.5 (s); 125.9 (d); 128.2 (s); 129.3 (d); 132.6 (s); 142.3 (s); 143.9 (s); 145.1 (d); 158.4 (s).
-
6, 75 MHz): 21.0 (q); 55.9 (q); 93.0 (d); 102.1 (d); 113.9 (s); 120.2 (d); 124.4 (d); 125.5 (s); 125.9 (d); 128.2 (s); 129.3 (d); 132.6 (s); 142.3 (s); 143.9 (s); 145.1 (d); 158.4 (s).
-
-
-
-
16
-
-
85031138070
-
-
3, 100 MHz) 21.9 (q); 25.3 (q); 56.2 (q); 93.9 (s); 94.1 (s); 102.5 (d, C3); 107.8 (d, C6); 117.3 (d, C5′); 129.0 (d, Ts); 129.5 (d, Ts); 136.3 (s); 136.5 (s); 140.1 (d, C7); 141.9 (s); 142.9 (d, C6′); 143.5 (s); 144.9 (s); 156.9 (d, 2); 158.5 (s); 160.4 (s); 162.0 (s).
-
3, 100 MHz) 21.9 (q); 25.3 (q); 56.2 (q); 93.9 (s); 94.1 (s); 102.5 (d, C3); 107.8 (d, C6); 117.3 (d, C5′); 129.0 (d, Ts); 129.5 (d, Ts); 136.3 (s); 136.5 (s); 140.1 (d, C7); 141.9 (s); 142.9 (d, C6′); 143.5 (s); 144.9 (s); 156.9 (d, 2); 158.5 (s); 160.4 (s); 162.0 (s).
-
-
-
-
17
-
-
85031137258
-
-
3, 100).
-
3, 100).
-
-
-
-
18
-
-
85031135311
-
-
3OD, 100 MHz) 20.1 (q); 101.8 (d, C3); 103.9 (s); 105.0 (s); 106.0 (d, C6); 110.1 (d, C5′); 123.5 (s); 128.0 (d, Ts); 128.9 (d, Ts); 129.3 (d, C7); 134.3 (d, C6′); 138.3 (s); 139.0 (s); 142.9 (s); 143.1 (s); 156.2 (s); 159.0 (s); 160.7 (d, C2).
-
3OD, 100 MHz) 20.1 (q); 101.8 (d, C3); 103.9 (s); 105.0 (s); 106.0 (d, C6); 110.1 (d, C5′); 123.5 (s); 128.0 (d, Ts); 128.9 (d, Ts); 129.3 (d, C7); 134.3 (d, C6′); 138.3 (s); 139.0 (s); 142.9 (s); 143.1 (s); 156.2 (s); 159.0 (s); 160.7 (d, C2).
-
-
-
-
21
-
-
0000882277
-
-
Andersen K.K., Bray D.D., Chumpradit S., Clark M.E., Habgood G.J., Hubbard C.D., Young K.M. J. Org. Chem. 56:1991;6508-6516.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 6508-6516
-
-
Andersen, K.K.1
Bray, D.D.2
Chumpradit, S.3
Clark, M.E.4
Habgood, G.J.5
Hubbard, C.D.6
Young, K.M.7
-
26
-
-
0001244052
-
-
11 with Na-naphthalene in THF at -78°C was N-deprotected in a 25% yield. The tricyclic derivative
-
Nagashima H., Ozaki N., Washiyama M., Itoh K. Tetrahedron Lett. 26:1985;657-660. The tricyclic derivative 11 with Na-naphthalene in THF at -78°C was N-deprotected in a 25% yield.
-
(1985)
Tetrahedron Lett.
, vol.26
, pp. 657-660
-
-
Nagashima, H.1
Ozaki, N.2
Washiyama, M.3
Itoh, K.4
-
29
-
-
85031142423
-
-
The synthetic product had identical spectroscopic data to those described for variolin B and showed identical TLC and HPLC behaviour as a sample of the natural product supplied by Pharma Mar.
-
The synthetic product had identical spectroscopic data to those described for variolin B and showed identical TLC and HPLC behaviour as a sample of the natural product supplied by Pharma Mar.
-
-
-
|