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0035937773
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M. Manifava, J. W. J. F. Thuring, Z.-Y. Lim, L. Packman, A. B. Holmes and N. T. Ktistakis, J. Biol. Chem., 2001, 276, 8987
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Manifava, M.1
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Ktistakis, N.T.6
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74
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17844405295
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K. E. Anderson, P. Lipp, M. Bootman, S. H. Ridley, J. Coadwell, L. Ronnstrand, J. Lennartsson, A. B. Holmes, G. F. Painter, J. Thuring, Z. Y. Lim, H. Erdjument-Bromage, A. Grewal, P. Tempst, L. R. Stephens and P. T. Hawkins, Curr. Biol., 2000, 10, 1403
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Anderson, K.E.1
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Lennartsson, J.7
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Thuring, J.10
Lim, Z.Y.11
Erdjument-Bromage, H.12
Grewal, A.13
Tempst, P.14
Stephens, L.R.15
Hawkins, P.T.16
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75
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0033607548
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R. K. McEwen, S. K. Dove, F. T. Cooke, G. F. Painter, A. B. Holmes, A. Shisheva, Y. Ohya, P. J. Parker and R. H. Michell, J. Biol. Chem., 1999, 274, 33905.
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J. Biol. Chem.
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McEwen, R.K.1
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Shisheva, A.6
Ohya, Y.7
Parker, P.J.8
Michell, R.H.9
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76
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0032578999
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L. Stephens, K. Anderson, D. Stokoe, H. Erdjument-Bromage, G. F. Painter, A. B. Holmes, P. R. J. Gaffney, C. B. Reese, F. McCormick, P. Tempst, J. Coadwell and P. T. Hawkins, Science, 1998, 279, 710
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(1998)
Science
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Stephens, L.1
Anderson, K.2
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Erdjument-Bromage, H.4
Painter, G.F.5
Holmes, A.B.6
Gaffney, P.R.J.7
Reese, C.B.8
McCormick, F.9
Tempst, P.10
Coadwell, J.11
Hawkins, P.T.12
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77
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-
0030799706
-
-
D. Stokoe, L. R. Stephens, T. Copeland, P. R. J. Gaffney, C. B. Reese, G. F. Painter, A. B. Holmes, F. McCormick and P. T. Hawkins, Science, 1997, 277, 567
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(1997)
Science
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-
Stokoe, D.1
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Reese, C.B.5
Painter, G.F.6
Holmes, A.B.7
McCormick, F.8
Hawkins, P.T.9
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78
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-
0029993517
-
-
S. R. James, C. P. Downes, R. Gigg, S. J. A. Grove, A. B. Holmes and D. R. Alessi, Biochem. J, 1996, 315, 709.
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(1996)
Biochem. J
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James, S.R.1
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Holmes, A.B.5
Alessi, D.R.6
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79
-
-
76849093692
-
-
Stereochemical representation: myo-inositol (Scheme 1), structures 1, 11-14 and 27-29 are meio-compounds. Structures 2-7, 15 and 17-19 refer to racemic compounds. Structures in Fig. 1, cores A-E, structures 8-10, 16, 20 and 30-110 refer to single enantiomers.
-
Stereochemical representation: myo-inositol (Scheme 1), structures 1, 11-14 and 27-29 are meio-compounds. Structures 2-7, 15 and 17-19 refer to racemic compounds. Structures in Fig. 1, cores A-E, structures 8-10, 16, 20 and 30-110 refer to single enantiomers.
-
-
-
-
80
-
-
37049079369
-
-
D. C. Billington, R. Baker, J. J. Kulagowski, I. M. Mawer, J. P. Vacca, S. J. Desolms and J. R. Huff, J. Chem. Soc., Perkin Trans. 1, 1989, 1423
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J. Chem. Soc., Perkin Trans. 1
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Billington, D.C.1
Baker, R.2
Kulagowski, J.J.3
Mawer, I.M.4
Vacca, J.P.5
Desolms, S.J.6
Huff, J.R.7
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82
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0000782595
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S. J. A. Grove, I. H. Gilbert, A. B. Holmes, G. F. Painter and M. L. Hill, Chem. Commun., 1997, 1633.
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(1997)
Chem. Commun.
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-
Grove, S.J.A.1
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Painter, G.F.4
Hill, M.L.5
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85
-
-
76849085157
-
-
Bruzik subsequently used camphor dimethyl acetal for the early resolution of myoinositol as a strategy for the synthesis of analogues of all eight naturally occurring PIPs. See reference 10 for more details.
-
Bruzik subsequently used camphor dimethyl acetal for the early resolution of myoinositol as a strategy for the synthesis of analogues of all eight naturally occurring PIPs. See reference 10 for more details.
-
-
-
-
86
-
-
0027116057
-
-
I. H. Gilbert, A. B. Holmes, M. J. Pestchanker and R. C. Young, Carbohydr. Res., 1992, 234, 117.
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Carbohydr. Res.
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Gilbert, I.H.1
Holmes, A.B.2
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Young, R.C.4
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87
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85018436243
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ed. J. J. Eisch, and R. B. King, Academic Press, New York
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Organometallic Syntheses, ed. J. J. Eisch, and R. B. King, Academic Press, New York, Vol.2, p. 137
-
Organometallic Syntheses
, vol.2
, pp. 137
-
-
-
89
-
-
76849103626
-
-
Synthesised from myo-inositol and deuterated triethyl orthoformate, see Electronic Supporting Information for more details.
-
Synthesised from myo-inositol and deuterated triethyl orthoformate, see Electronic Supporting Information for more details.
-
-
-
-
90
-
-
69549116405
-
-
M. K. Johns, M.-X. Yin, S. J. Conway, D. E. J. E. Robinson, L. S.-M. Wong, R. Bamert, R. E. H. Wettenhall and A. B. Holmes, Org. Biomol. Chem., 2009, 7, 3691.
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Org. Biomol. Chem.
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-
Johns, M.K.1
Yin, M.-X.2
Conway, S.J.3
Robinson, D.E.J.E.4
Wong, L.S.-M.5
Bamert, R.6
Wettenhall, R.E.H.7
Holmes, A.B.8
-
92
-
-
76849110122
-
-
These compounds are notoriously difficult to characterise because of problems with solubility and/or micelle formation (also see reference 19). Characterisation data is available in the Electronic Supporting Information.
-
These compounds are notoriously difficult to characterise because of problems with solubility and/or micelle formation (also see reference 19). Characterisation data is available in the Electronic Supporting Information.
-
-
-
-
93
-
-
76849105094
-
-
1H NMR analysis of the supernatant (reference 12) or Biocore analysis (reference 29).
-
1H NMR analysis of the supernatant (reference 12) or Biocore analysis (reference 29).
-
-
-
-
95
-
-
0028439227
-
-
T. Desai, J. Gigg, R. Gigg, E. Martin-Zamora and N. Schnetz, Carbohydr. Res., 1994, 258, 135.
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-
Desai, T.1
Gigg, J.2
Gigg, R.3
Martin-Zamora, E.4
Schnetz, N.5
-
96
-
-
76849105823
-
-
Synthesised in a similar manner to dipalmitoyl phosphoramidite 34, see Electronic Supporting Information.
-
Synthesised in a similar manner to dipalmitoyl phosphoramidite 34, see Electronic Supporting Information.
-
-
-
-
97
-
-
76849091944
-
-
Phosphoramidite 104 was synthesised from 35 following the procedure for the synthesis of 38, see Electronic Supporting Information for more details.
-
Phosphoramidite 104 was synthesised from 35 following the procedure for the synthesis of 38, see Electronic Supporting Information for more details.
-
-
-
-
98
-
-
50249084987
-
-
E. L. Axe, S. A. Walker, M. Manifava, P. Chandra, H. L. Roderick, A. Habermann, G. Griffiths and N. T. Ktistakis, J. Cell Biol., 2008, 182, 685.
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J. Cell Biol.
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-
Axe, E.L.1
Walker, S.A.2
Manifava, M.3
Chandra, P.4
Roderick, H.L.5
Habermann, A.6
Griffiths, G.7
Ktistakis, N.T.8
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