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85022595277
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For reviews see: (a) Lautens, M. Synlett 1993, 177.
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Lautens, M.1
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4
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0037239379
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For a review of the ring opening methodologies developed in our labs see: Lautens, M.; Fagnou, K.; Hiebert, S. Acc. Chem. Res. 2003, 36, 48.
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7
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0002063517
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For other examples of enantioselective alkylative ring opening of oxabicycles see: (a) Lautens, M.; Gadja, C.; Chiu, P. J. Chem. Soc., Chem. Commun. 1993, 1193.
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0001701335
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0031573812
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19
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0000563324
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Lautens, M.1
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20
-
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0033575073
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Synthesized as in: Fujii, A.; Hagiwara, E.; Sodeoka, M. J. Am. Chem. Soc. 1999, 121, 5450.
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-
24
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-
1042293868
-
-
note
-
For details on the synthesis and use of these reagents see the Supporting Information.
-
-
-
-
25
-
-
1042305489
-
-
note
-
The enantiomeric excess of 30, 31, and 27 (entries 5 and 8) were all determined to be 98%. The enantiomeric excess of these products is determined in the carbopalladation step leading to intermediate iv.
-
-
-
-
27
-
-
0004228992
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Taylor, R. J. K., Ed.; Oxford University Press: Oxford
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Knochel, P.1
Rozema, M.J.2
Tucker, C.E.3
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28
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0037111797
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Lautens, M.1
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29
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0000299234
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Lautens, M.; Dockendorff, C.; Fagnou, K.; Malicki, A. Org. Lett. 2002, 4, 1311.
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Lautens, M.1
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30
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0001827627
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Miyaura, N.; Tanabe, Y.; Suginome, H.; Suzuki, A. J. Organomet. Chem. 1982, 233, C13.
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32
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33748241772
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33
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0000989934
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-
34
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0000836984
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(b) Bolm, C.; Ewald, M.; Felder, M. Chem. Ber. 1992, 125, 1205.
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Bolm, C.1
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-
35
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0025965025
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-
36
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0033960441
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Spieler, J.1
Huttenloch, O.2
Waldman, H.3
-
39
-
-
1042270750
-
-
note
-
For details see the Supporting Information.
-
-
-
-
40
-
-
1042270751
-
-
note
-
2Zn of 0.25 M.
-
-
-
-
41
-
-
1042293867
-
-
note
-
Spectral data reported for the mixture.
-
-
-
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