-
1
-
-
0000249280
-
-
and references therein
-
(a) Banfield, J. E.; Black, D. St. C.; Johns, S. R.: Willing, R. I. Aust. J. Chem. 1982, 35, 2247 and references therein.
-
(1982)
Aust. J. Chem.
, vol.35
, pp. 2247
-
-
Banfield, J.E.1
Black, D.St.C.2
Johns, S.R.3
Willing, R.I.4
-
3
-
-
0034898137
-
-
(a) Kurosawa, K.; Takahashi, K.; Tsuda, E. J. Antibiot. 2001, 54, 541.
-
(2001)
J. Antibiot.
, vol.54
, pp. 541
-
-
Kurosawa, K.1
Takahashi, K.2
Tsuda, E.3
-
4
-
-
0034904357
-
-
(b) Takahashi, K.; Tsuda, E.; Kurosawa, K. J. Antibiot. 2001, 54, 548.
-
(2001)
J. Antibiot.
, vol.54
, pp. 548
-
-
Takahashi, K.1
Tsuda, E.2
Kurosawa, K.3
-
5
-
-
11144327147
-
-
(a) Manzo, E.; Ciavatta, M. L.; Gavagnin, M.; Mollo, E.; Wahidulla, S.; Cimino, G. Tetrahedron Lett. 2005, 46, 465.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 465
-
-
Manzo, E.1
Ciavatta, M.L.2
Gavagnin, M.3
Mollo, E.4
Wahidulla, S.5
Cimino, G.6
-
6
-
-
32744457466
-
-
in press
-
The correct structure of compound 5 was reassigned by total synthesis: (b) Miller, A. K.; Trauner. D. Angew. Chem., Int. Ed. 2005, in press. We propose to call 5 and 6 ocellapyrones A and B respectively.
-
(2005)
Angew. Chem., Int. Ed.
-
-
Miller, A.K.1
Trauner, D.2
-
7
-
-
13844276169
-
-
Cueto, M.; D'Croz, L.; Maté, J. L.; San-Martín, A.; Darias, J. Org. Lett. 2005, 7, 415.
-
(2005)
Org. Lett.
, vol.7
, pp. 415
-
-
Cueto, M.1
D'Croz, L.2
Maté, J.L.3
San-Martín, A.4
Darias, J.5
-
9
-
-
0037126282
-
-
(b) Moses, J. E.; Baldwin, J. E.; Marquez, R.; Adlington; R. M.; Cowley, A. R. Org. Lett. 2002, 4, 3731.
-
(2002)
Org. Lett.
, vol.4
, pp. 3731
-
-
Moses, J.E.1
Baldwin, J.E.2
Marquez, R.3
Adlington, R.M.4
Cowley, A.R.5
-
10
-
-
14844362283
-
-
(c) Jacobsen, M. F.; Moses, J. E.; Adlington, R. M.; Baldwin, J. E. Org. Lett. 2005, 7, 641.
-
(2005)
Org. Lett.
, vol.7
, pp. 641
-
-
Jacobsen, M.F.1
Moses, J.E.2
Adlington, R.M.3
Baldwin, J.E.4
-
13
-
-
0000506480
-
-
Beak, P.; Lee, J. K.; Mckinnie, B. G. J. Org. Chem. 1978, 43, 1367.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 1367
-
-
Beak, P.1
Lee, J.K.2
Mckinnie, B.G.3
-
14
-
-
32744461310
-
-
See ref 3b
-
Compound 13 has also been made by Baldwin et al. through a different route in the context of a synthesis of 5. See ref 3b.
-
-
-
-
15
-
-
0000089016
-
-
Ashe, A. J., III; Lohr, L. L.; Al-Tawell, S. M. Organometallics 1991, 10, 2424.
-
(1991)
Organometallics
, vol.10
, pp. 2424
-
-
Ashe III, A.J.1
Lohr, L.L.2
Al-Tawell, S.M.3
-
16
-
-
1842565056
-
-
Mee, S. P. H.; Lee, V.; Baldwin, J. Angew. Chem., Int. Ed. 2004, 43, 1132.
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1132
-
-
Mee, S.P.H.1
Lee, V.2
Baldwin, J.3
-
17
-
-
32744467087
-
-
note
-
Compound 22 was obtained under these conditions together with varying amounts (20-35%) of inseparable compound 21. The reason for this contamination is under investigation.
-
-
-
-
19
-
-
0001459493
-
-
Suzuki, M.; Ohtake, H.; Kameya, Y.; Hamanaka, N.; Noyori, R. J. Org. Chem. 1989, 54, 5292.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 5292
-
-
Suzuki, M.1
Ohtake, H.2
Kameya, Y.3
Hamanaka, N.4
Noyori, R.5
|