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1b
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2
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5b
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12 Macrodiolide 12: [α]
d
+40.5
(c 2, CHCl3); IR (neat): nmax = 1735,
1666, 1633 and 1591 cm-¹; ¹H
NMR (400 MHz, CDCl3): δ = 1.34 (6 H,
d, J = 6.4 Hz, 2 × CH3),
2.44 (2 H, dddd, J = 15.0, 7.0,
3.5, 1.0 Hz, 8-HH and 8′-HH), 2.67 (2 H, dddd, J = 15.0,
9.3, 7.8, 1.0 Hz, 8-HH and 8′-HH), 3.54 (2 H, d, J = 15.0
Hz, 2-HH and 2′-HH), 3.60 (2 H, d, J = 15.0
Hz, 2-HH and 2′-HH), 5.10 (2 H, m, 9-H and 9′-H),
5.96 (2 H, m, 7-H and 7′-H), 6.11 (2 H, d, J = 15.5 Hz, 4-H and 4′-H), 6.24
(2 H, t, J = 11.5 Hz, 6-H and
6′-H), 7.45 (2 H, ddd, J = 15.5,
11.5, 1.0 Hz, 5-H and 5′-H); ¹³C
NMR (100 MHz, CDCl3): δ = 19.8 (2 × CH3),
34.6 (C-8 and C-8′), 47.6 (C-2 and C-2′), 70.8
(C-9 and C-9′), 129.3 (C-4 and C-4′), 130.1 (C-6
and C-6′), 136.8 (C-7 and C-7′), 138.8 (C-5 and
C-5′), 166.9 (C-1 and C-1′) and 191.9 (C-3 and
C-3′); MS (CI):
m/z = 361.1652 (MH+,
C20H25O6 requires 361.1651), 361 (MH+,
100%) and 181 (99).
13a
Booth PM.
Broughton HB.
Ford MJ.
Fox CMJ.
Ley SV.
Slawin AMZ.
Williams DJ.
Woodward PR.
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1989,
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7565
13b
Lobell M.
Schneider MP.
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1993,
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1027
13c
Nagahara K.
Ryu I.
Yamazaki H.
Kambe N.
Komatsu M.
Sonoda N.
Baba A.
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1997,
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14
Mckay C.
Simpson TJ.
Willis CL.
Forrest AK.
O’Hanlon PJ.
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15 Macrodiolide 16: [α]
d
+ 124 (c 1, CHCl3); IR (neat): nmax = 1732,
1673, 1627 cm-¹; ¹H
NMR (400 MHz, CDCl3): δ = 1.24 (6 H,
d, J = 6.4 Hz, 2 × CH3),
1.40-1.65 (8 H, m, 7-H2, 7′-H2, 8-H2 and
8′-H2), 2.20 (4 H, m, 6-H2 and 6′-H2),
3.52 (2 H, d, J = 14.0 Hz, 2-HH and 2′-HH),
3.57 (2 H, d, J = 14.0 Hz, 2-HH and 2′-HH), 4.97 (2 H, m, 9-H and 9′-H),
6.13 (2 H, dt, J = 16.0, 1.5
Hz, 4-H and 4′-H), 6.86 (2 H, dt, J = 16.0, 6.5
Hz, 5-H and 5′-H); ¹³C NMR
(100 MHz, CDCl3): δ = 20.0 (2 × CH3),
23.7 (C-7 and C-7′), 32.2 (C-6 and C-6′), 35.2
(C-8 and C-8′), 47.3 (C-2 and C-2′), 71.5 (C-9
and C-9′), 129.1 (C-4 and C-4′), 148.5 (C-5 and
C-5′), 165.8 (C-1 and C-1′) and 190.7 (C-3 and
C-3′); MS (EI): m/z = 364.1879 (M+,
C20H28O6 requires 364.1886), 364
(M+, 5%), 182 (50) and 81 (100).