Chemistry Reference
In-Depth Information
37. Van Veldhuizen , J. J. ; Campbell , J. E. ; Giudici , R. E. ; Hoveyda , A. H. J. Am. Chem. Soc. 2005 , 127 ,
6877 - 6882 .
38. Berlin , J. M. ; Goldberg , S. D. ; Grubbs , R. H. Angew. Chem. Int. Ed. 2006 , 45 , 7591 - 7595 .
39. Gillingham , D. G. ; Kataoka , O. ; Garber , S. B. ; Hoveyda , A. H. J. Am. Chem. Soc. 2004 , 126 ,
12288 - 12290 .
40. Cortez , G. A. ; Baxter , C. A. ; Schrock , R. R. ; Hoveyda , A. H. Org. Lett. 2007 , 9 , 2871 - 2874 .
41. Endo - substituted
[3.2.1] - bicycles
are
typically
more
reactive
than
the
corresponding
exo -
diastereomers due to increased ring strain.
42. For discussions regarding enantioselective formation of C - halogen bonds; see: (a) Ibrahim , H. ; Togni ,
A . Chem. Comm. 2004 , 1147 - 1155 . (b) Gaunt , M. J. ; Johansson , C. C. Chem. Rev. 2007 , 107 , 5596 -
5605 . (c) Sakakura , A. ; Ukai , A. ; Ishihara , K. Nature 2007 , 445 , 900 - 903 . (d) Kotsuki , H. ; Ikishima ,
H. ; Okuyama , A. Heterocycles 2008 , 75 , 757 - 797 .
43. Gillingham , D. G. ; Hoveyda , A. H. Angew. Chem. Int. Ed. 2007 , 46 , 3860 - 3864 .
44. Cortez , G. A. ; Schrock , R. R. ; Hoveyda , A. H. Angew. Chem. Int. Ed. 2007 , 46 , 4534 - 4538 .
45. This concept has been applied to the synthesis of azabicycles through ring-closing metathesis; see:
Neipp , C. E. ; Martin , S. F. J. Org. Chem. 2003 , 68 , 8867 - 8878 .
46. Although Mo complex 1b affords
>
98% conversion, the desired products are obtained in
<
2% ee. All
other Mo catalysts fail to deliver the desired product (
<
2% conversion).
47. Maison ,
W. ;
B ü chert ,
M. ;
Deppermann ,
N.
Beilstein J. Org. Chem.
2007 ,
3
(DOI:
10.1186/1860 - 5397 - 3 - 48).
48. Giudici , R. E. ; Hoveyda , A. H. J. Am. Chem. Soc. 2007 , 129 , 3824 - 3825 .
49. (a) Bornand , M. ; Chen , P. Angew. Chem. Int. Ed. 2005 , 44 , 7909 - 7911 . (b) Bornand , M. ; Torker , S. ;
Chen , P. Organometallics 2007 , 26 , 3585 - 3596 .
50. The r value is a mathematical description of the sequence selectivity of the alternating copolymeriza-
tion; see: Polic , A. L. ; Duever , T. A. ; Penlidis , A. J. Polym. Sci. A 1998 , 36 , 813 - 822 .
51. For a review of catalytic cross - metathesis reactions, see: Connon , S. J. ; Blechert , S. Angew. Chem. Int.
Ed. 2003 , 42 , 1900 - 1923 .
52. For a review of catalytic enyne metathesis reactions, see: Diver , S. T. ; Giessert , A. J. Chem. Rev. 2004 ,
104 , 1317 - 1382 .
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