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DOI: 10.1055/s-0029-1218538
Total Synthesis of (+)-Cephalosporolide E and (-)-Cephalosporolide F en route to Bassianolone
Publication History
Publication Date:
01 December 2009 (online)
Abstract
A stereoselective synthesis of (+)-cephalosporolide E and (-)-cephalosporolide F en route to bassianolone is described. The key steps involve cross metathesis to get the desired β,γ-unsaturated ester, asymmetric dihydroxylation to install the β-hydroxy-γ-lactone moiety and spiroketalization. Although attempts to get free bassianolone failed, the first total synthesis of natural cephalosporolides E and F has been achieved in nine steps and 6.3% and 3.5% overall yields, respectively.
Key words
bassianolone - cephalosporolides - cross metathesis - asymmetric dihydroxylation - spiroketalization
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References and Notes
¹H NMR and ¹³C
NMR studies of purified product indicated single diastereomer.
Data for 18
Colourless oil; [α]D
²5 +10.2
(c 0.2, CHCl3). IR (CHCl3): ν = 3463,
3022, 2973, 1772, 1646, 1528, 1421, 1347, 1216, 1045, 927, 669 cm-¹. ¹H
NMR (400 MHz, CDCl3/TMS): δ = 0.02
(s, 3 H), 0.03 (s, 3 H), 0.86 (s, 9 H), 1.11 (d, J = 6.1 Hz,
3 H), 1.43-1.49 (m, 2 H), 1.50-1.58 (m, 1 H),
1.72-1.80 (m, 1 H), 2.24-2.37 (m, 2 H), 2.54 (d, J = 17.7 Hz,
1 H), 2.72 (dd, J = 17.7,
5.8 Hz, 1 H), 3.44 (br s, OH), 3.75-3.80 (m, 1 H), 3.93-4.02
(m, 4 H), 4.36-4.38 (m, 1 H), 4.55-4.60 (m, 1 H). ¹³C
NMR (100 MHz, CDCl3): δ = -4.83, -4.39,
18.0, 23.6, 25.7 (3 C), 32.7, 33.7, 34.1, 37.7, 64.1, 64.5, 67.9,
68.3, 80.9, 110.1, 175.3. HRMS (ESI-TOF): m/z calcd
for C18H34O6Si + Na: 397.2022;
found: 397.2028.
Data for 19
Colourless
oil; [α]D
²5 -20.4
(c 0.1, CHCl3). IR (CHCl3): ν = 3440,
3018, 2965, 2931, 1773, 1636, 1458, 1407, 1378, 1216, 1160, 1062,
949, 668 cm-¹. ¹H
NMR (400 MHz, CDCl3/TMS): δ = 1.21
(d, J = 6.4
Hz, 3 H), 1.47-1.57 (m, 2 H), 1.79-1.87 (m, 2
H), 2.33-2.36 (m, 2 H), 2.56 (d, J = 17.7 Hz,
1 H), 2.76 (dd, J = 17.8,
5.9 Hz, 1 H), 3.36-3.45 (br s, OH), 3.78-3.82
(m, 1 H), 3.98-4.06 (m, 4 H), 4.39-4.41 (m, 1
H), 4.56-4.61 (m, 1 H). ¹³C
NMR (100 MHz, CDCl3): δ = 23.6,
33.3 (2 C), 34.3, 37.9, 64.3, 64.7, 67.6, 68.5, 81.1, 110.1, 175.5.
HRMS (ESI-TOF): m/z calcd for
C12H20O6 + H: 261.1338;
found: 261.1341.