-
1
-
-
0034680167
-
-
C. Walsh Nature 406 2006 775 781
-
(2006)
Nature
, vol.406
, pp. 775-781
-
-
Walsh, C.1
-
5
-
-
22544485071
-
-
A.L. Piccinelli, O. Cuesta-Rubio, M.B. Chica, N. Mahmood, B. Pagano, M. Pavone, V. Barone, and L. Rastrelli Tetrahedron 61 2005 8206 8211
-
(2005)
Tetrahedron
, vol.61
, pp. 8206-8211
-
-
Piccinelli, A.L.1
Cuesta-Rubio, O.2
Chica, M.B.3
Mahmood, N.4
Pagano, B.5
Pavone, M.6
Barone, V.7
Rastrelli, L.8
-
6
-
-
0346035902
-
-
C. Ito, M. Itoigawa, Y. Miyamoto, S. Onoda, K.S. Rao, T. Mukainaka, H. Tokuda, H. Nishino, and H. Furukawa J. Nat. Prod. 66 2003 206 209
-
(2003)
J. Nat. Prod.
, vol.66
, pp. 206-209
-
-
Ito, C.1
Itoigawa, M.2
Miyamoto, Y.3
Onoda, S.4
Rao, K.S.5
Mukainaka, T.6
Tokuda, H.7
Nishino, H.8
Furukawa, H.9
-
9
-
-
78650385280
-
-
E.H. Krenske, K.N. Houk, D. Lim, S.E. Wengryniuk, and D.M. Coltart J. Org. Chem. 75 2010 8578 8584
-
(2010)
J. Org. Chem.
, vol.75
, pp. 8578-8584
-
-
Krenske, E.H.1
Houk, K.N.2
Lim, D.3
Wengryniuk, S.E.4
Coltart, D.M.5
-
12
-
-
33845249441
-
-
For previous racemic syntheses of clusianone, see: (a)
-
For previous racemic syntheses of clusianone, see: (a) V. Rodeschini, N.M. Ahmad, and N.S. Simpkins Org. Lett. 8 2006 5283 5285
-
(2006)
Org. Lett.
, vol.8
, pp. 5283-5285
-
-
Rodeschini, V.1
Ahmad, N.M.2
Simpkins, N.S.3
-
14
-
-
34250836871
-
-
N.M. Ahmad, V. Rodeschini, N.S. Simpkins, S.E. Ward, and A.J. Blake J. Org. Chem. 72 2007 4803 4815
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4803-4815
-
-
Ahmad, N.M.1
Rodeschini, V.2
Simpkins, N.S.3
Ward, S.E.4
Blake, A.J.5
-
16
-
-
33846570462
-
-
P. Nuhant, M. David, T. Pouplin, B. Delpech, and C. Marazano Org. Lett. 9 2007 287 289
-
(2007)
Org. Lett.
, vol.9
, pp. 287-289
-
-
Nuhant, P.1
David, M.2
Pouplin, T.3
Delpech, B.4
Marazano, C.5
-
18
-
-
34249784845
-
-
For previous asymmetric syntheses of clusianone, see: (a)
-
For previous asymmetric syntheses of clusianone, see: (a) V. Rodeschini, N.S. Simpkins, and C. Wilson J. Org. Chem. 72 2007 4265 4267
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4265-4267
-
-
Rodeschini, V.1
Simpkins, N.S.2
Wilson, C.3
-
21
-
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84929963399
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Simple modifications to PPAP ring structures have been shown to have a large effect on their biological activity. See, for example, Ref. 3.
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Simple modifications to PPAP ring structures have been shown to have a large effect on their biological activity. See, for example, Ref. 3.
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23
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84929949263
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Refs. 6,8, and unpublished results
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Refs. 6,8, and unpublished results.
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24
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84929964629
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Established by HPLC using a chiral, non-racemic stationary phase by comparison to an independently prepared racemic sample of 16 under conditions that gave baseline separation of its enantiomers (see Ref. 6 for details)
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Established by HPLC using a chiral, non-racemic stationary phase by comparison to an independently prepared racemic sample of 16 under conditions that gave baseline separation of its enantiomers (see Ref. 6 for details).
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