References and Notes
<A NAME="RW20610ST-1">1</A>
Yang SP.
Gao ZB.
Wang FD.
Liao SG.
Chen
HD.
Zhang CR.
Hu GY.
Yue JM.
Org.
Lett.
2007,
9:
903
<A NAME="RW20610ST-2">2</A>
Liu Y.
Nan FJ.
Tetrahedron Lett.
2010,
51:
1374
<A NAME="RW20610ST-3A">3a</A>
Deng LS.
Ma ZX.
Zhang YZ.
Zhao G.
Synlett
2007,
87
<A NAME="RW20610ST-3B">3b</A>
Deng LS.
Ma ZX.
Zhao G.
Synlett
2008,
728
<A NAME="RW20610ST-3C">3c</A>
Ye ZQ.
Deng LS.
Qian S.
Zhao G.
Synlett
2009,
2469
<A NAME="RW20610ST-3D">3d</A>
Wu H.
Zhang HL.
Zhao G.
Tetrahedron
2007,
63:
6454
<A NAME="RW20610ST-4">4</A>
Kwabata J.
Fukushi Y.
Tahara S.
Mizutani J.
Phytochemistry
1990,
29:
2332
<A NAME="RW20610ST-5A">5a</A>
Micheli RA.
Hajos ZG.
Cohen N.
Parrish DR.
Portland LA.
Sciamanna W.
Scott MA.
Wehrli PA.
J. Org. Chem.
1975,
40:
675
<A NAME="RW20610ST-5B">5b</A>
Isaacs RCA.
Grandi MJD.
Danishefsky SJ.
J. Org. Chem.
1993,
58:
3938 ; and references therein
<A NAME="RW20610ST-6A">6a</A>
Corey EJ.
Huang AX.
J.
Am. Chem. Soc.
1999,
121:
710
<A NAME="RW20610ST-6B">6b</A>
Daniewski AR.
Kiegiel J.
J. Org.
Chem.
1988,
53:
5534
<A NAME="RW20610ST-7">7</A>
Hwu JR.
Wetzel JM.
J. Org. Chem.
1985,
50:
3946
<A NAME="RW20610ST-8">8</A>
Ito Y.
Hirao T.
Saegusa T.
J. Org.
Chem.
1978,
43:
1011
<A NAME="RW20610ST-9">9</A>
Yadav VK.
Kapoor KK.
Tetrahedron
1995,
51:
8573
<A NAME="RW20610ST-10A">10a</A>
Hoveyda AH.
Evans DA.
Fu GC.
Chem.
Rev.
1993,
93:
1307
<A NAME="RW20610ST-10B">10b</A>
Lebel H.
Marcoux JF.
Molinaro C.
Charette AB.
Chem. Rev.
2003,
103:
977
<A NAME="RW20610ST-11">11</A>
Wharton PS.
Bohlen DH.
J. Org. Chem.
1961,
26:
3615
<A NAME="RW20610ST-12">12</A>
Grandi MJD.
Coburn CA.
Isaacs RCA.
Danishefsky SJ.
J. Org. Chem.
1993,
58:
7728
<A NAME="RW20610ST-13">13</A>
Charette AB.
Lebel H.
J. Org. Chem.
1995,
60:
2966
<A NAME="RW20610ST-14">14</A>
The same operative procedure should
be conducted to ensure that the starting material is completely
consumed. For details, see the Supporting Information.
<A NAME="RW20610ST-15">15</A>
See the Supporting Information for
details. CCDC 804060 (4) and 804061 (14) contain the supplementary crystallogra-phic
data for this paper. These data can be obtained free of charge from
The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
<A NAME="RW20610ST-16">16</A>
Thompson CF.
Jamison TF.
Jacobsen EN.
J. Am. Chem. Soc.
2000,
122:
10482
<A NAME="RW20610ST-17A">17a</A>
Nair V.
Sinhababu A.
J.
Org. Chem.
1978,
43:
5013
<A NAME="RW20610ST-17B">17b</A>
Caglioti L.
Tetrahedron
1966,
22:
487
<A NAME="RW20610ST-18">18</A>
Dess DB.
Martin JC.
J. Org. Chem.
1983,
48:
4155
<A NAME="RW20610ST-19">19</A>
Tatsuta K.
Shohei Y.
Kurihara K.
Tanabe K.
Shinei R.
Okonogi T.
Tetrahedron Lett.
1997,
38:
1439
<A NAME="RW20610ST-20">20</A>
Data of the Core
Fragment 4
[α]D
²8 56.2
(c 0.12, CHCl3); mp 133-135 ˚C.
IR (film): 2921, 2850, 1735, 1464, 1374, 1265, 1045 cm-¹. ¹H
NMR (400 MHz, CDCl3): δ = 6.16 (s,
1 H), 4.39 (t, J = 5.2
Hz, 1 H), 2.60-2.40 (m, 2 H), 2.20-2.10 (m, 1
H), 1.89 (s, 3 H), 1.80-1.65 (m, 1 H), 1.65-1.50
(m, 1 H), 1.30-1.20 (m, 1 H), 1.09 (s, 3 H), 0.91 (s, 9
H), 1.80-1.65 (m, 1 H), 0.10 (s, 3 H), 0.07 (s, 3 H). ¹³C
NMR (100 MHz, CDCl3): δ = 171.2, 149.4, 149.3,
122.1, 121.0, 72.9, 61.9, 42.1, 29.1, 26.2, 25.8, 23.3, 21.4, 18.2,
12.1, 8.5, -4.7, -5.3. ESI-MS: m/z = 369.2 [M + Na]+.
ESI-HRMS: m/z calcd for C20H30O3SiNa+ [M + Na]+: 369.1862;
found: 369.1856.