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80755158091
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De Meijere, A., Ed.; Thieme: Stuttgart
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84981772814
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57549108561
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8
-
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0000962519
-
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corrigendum, 3523
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-
Corey, E.J.1
Yamamoto, H.2
-
11
-
-
0040552001
-
-
For examples (target and yield for allylic alcohol indicated), see:;;;, [JH-I, 60%]
-
For examples (target and yield for allylic alcohol indicated), see: Corey, E. J.; Yamamoto, H.; Herron, D. K.; Achiwa, K. J. Am. Chem. Soc. 1970, 92, 6635-6636 [JH-I, 60%].
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-
Corey, E.J.1
Yamamoto, H.2
Herron, D.K.3
Achiwa, K.4
-
12
-
-
0001101383
-
-
[JH-I, 50%]
-
Corey, E. J.; Yamamoto, H. J. Am. Chem. Soc. 1970, 92, 6636-6637 [JH-I, 50%].
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J. Am. Chem. Soc.
, vol.92
, pp. 6636-6637
-
-
Corey, E.J.1
Yamamoto, H.2
-
13
-
-
0001243026
-
-
[farnesol, 46%]
-
Corey, E. J.; Yamamoto, H. J. Am. Chem. Soc. 1970, 92, 6637-6638 [farnesol, 46%].
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(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 6637-6638
-
-
Corey, E.J.1
Yamamoto, H.2
-
14
-
-
0017372091
-
-
[8- epi -dendrobine, 40%]
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Borch, R. F.; Evans, A. J.; Wade, J. J. J. Am. Chem. Soc. 1977, 99, 1612-1619 [8- epi -dendrobine, 40%].
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-
Borch, R.F.1
Evans, A.J.2
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15
-
-
0000652590
-
-
[nuciferol, 42%]
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Takano, S.; Goto, E.; Ogasawara, K. Tetrahedron Lett. 1982, 23, 5567-5570 [nuciferol, 42%].
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Takano, S.1
Goto, E.2
Ogasawara, K.3
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16
-
-
77956593128
-
-
[manwuweizic acid, 54%]
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Liu, J.-S.; Tao, Y. Tetrahedron 1992, 48, 6193-6798 [manwuweizic acid, 54%].
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Tetrahedron
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Liu, J.-S.1
Tao, Y.2
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17
-
-
0043029011
-
-
[iricinin-4, 40%]
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Fuörstner, A.; Gastner, T.; Rust, J. Synlett 1999, 29-32 [iricinin-4, 40%].
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, pp. 29-32
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Fuörstner, A.1
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Rust, J.3
-
18
-
-
4344568706
-
-
[mispyric acid, 22%]
-
Imamura, Y.; Takikawa, H.; Sasaki, M.; Mori, K. Org. Biomol. Chem. 2004, 2, 2236-2244 [mispyric acid, 22%]
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Imamura, Y.1
Takikawa, H.2
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Mori, K.4
-
19
-
-
0001474258
-
-
2
-
2: Sosnovsky, G.; Rao, N. U. M.; Li, S. W.; Swartz, H. M. J. Org. Chem. 1989, 54, 3667-3674
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-
Sosnovsky, G.1
Rao, N.U.M.2
Li, S.W.3
Swartz, H.M.4
-
20
-
-
77956589625
-
-
All yields reported are for chromatographically purified products. All E / Z ratios reported were determined on crude reaction mixtures by GC/MS. E / Z assignments were based on NOE studies
-
All yields reported are for chromatographically purified products. All E / Z ratios reported were determined on crude reaction mixtures by GC/MS. E / Z assignments were based on NOE studies.
-
-
-
-
21
-
-
77956599194
-
-
Chloromethyl acetate gave the allylic acetate 6a in 71% yield, >99% Z
-
Chloromethyl acetate gave the allylic acetate 6a in 71% yield, >99% Z.
-
-
-
-
22
-
-
64549126511
-
-
For a review on allylic alcohols, see:; Clayden, J., Ed.; Thieme: Stuttgart
-
For a review on allylic alcohols, see: Hodgson, D. M.; Humphreys, P. G. In Science of Synthesis; Clayden, J., Ed.; Thieme: Stuttgart, 2007; Vol. 32, pp 583 - 665.
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Hodgson, D.M.1
Humphreys, P.G.2
Clayden, J.3
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25
-
-
33847799798
-
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Ireland, R. E.; Mueller, R. H.; Willard, A. K. J. Am. Chem. Soc. 1976, 98, 2868-2877
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Ireland, R.E.1
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26
-
-
4344610661
-
-
For a review, see
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For a review, see: Martín Castro, A. M. Chem. Rev. 2004, 104, 2939-3002
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, pp. 2939-3002
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Martín Castro, A.M.1
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27
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41649084196
-
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See also
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See also: Fleming, F. F.; Liu, W.; Ghosh, S.; Steward, O. M. J. Org. Chem. 2008, 73, 2803-2810
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Fleming, F.F.1
Liu, W.2
Ghosh, S.3
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28
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34250735074
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Gao, X.; Lin, C.-J.; Jia, Z.-J. J. Nat. Prod. 2007, 70, 830-834
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Gao, X.1
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29
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33947279305
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Kong, L.; Zhuang, Z.; Chen, Q.; Deng, H.; Tang, Z.; Jia, X.; Li, Y.; Zhai, H. Tetrahedron: Asymmetry 2007, 18, 451-454
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Kong, L.1
Zhuang, Z.2
Chen, Q.3
Deng, H.4
Tang, Z.5
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Li, Y.7
Zhai, H.8
-
30
-
-
0032715231
-
-
Mikami, K.; Koizumi, Y.; Osawa, A.; Terada, M.; Takayama, H.; Nakagawa, K.; Okano, T. Synlett 1999, 1899-1902
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Mikami, K.1
Koizumi, Y.2
Osawa, A.3
Terada, M.4
Takayama, H.5
Nakagawa, K.6
Okano, T.7
-
31
-
-
77956584449
-
-
See Supporting Information for details
-
See Supporting Information for details.
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