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8
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10
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0004171091
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12
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0343655273
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note
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2OAc: 4.02-4.07 (2H, t, J=6.8-7.2 Hz) and MeCO 1.96-2.06 (3H, s) (for 4a, 5a, 6a, 9a).
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13
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0000696063
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Ibata, K.; Mizuno, M.; Tanaka, Y.; Kageyu, A. Phytochemistry 1984, 23, 783.
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Ibata, K.1
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Kageyu, A.4
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15
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0001306618
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Quite recently the use of a similar approach was reported in a preliminary form for ω-end functionalization of all-E-octaprenyl acetate:
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Quite recently the use of a similar approach was reported in a preliminary form for ω-end functionalization of all-E-octaprenyl acetate: Handa, S.; Pattenden, G. J. Chem. Soc. Perkin Trans. 1 1999, 843.
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J. Chem. Soc. Perkin Trans. 1
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Handa, S.1
Pattenden, G.2
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16
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0343655272
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note
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2C(Me)=), 125.1 (HC=), 135.3 (C(Me)=). The corresponding signals of the E-isoprene units are at δ 16.0, 26.7, 39.9, 124.3 and 134.8, those of α-terminal dihydroisoprene unit are at δ 19.5 (MeCH), 29.3 (C3), 37.4 (C4), 39.7 (C2), and 61.2 (C1). Some of the main signals of internal isoprene units shown are accompanied by groups of more weak signals due to influence of the stereochemistry of neighboring isoprene units. The characteristic signals of naphtalene fragment in 10c are at δ 104.2, 117.1, 119.8, 128.7 and 143.6, other signals are close to signals of HC= and C(Me)= atoms of internal isoprene units.
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17
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0024807186
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Danilov L.L., Druzhinina T.N., Kalinchuk N.A., Maltsev S.D., Shibaev V.N. Chem. Phys. Lipids. 51:1989;191.
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Danilov, L.L.1
Druzhinina, T.N.2
Kalinchuk, N.A.3
Maltsev, S.D.4
Shibaev, V.N.5
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18
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0001888574
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Atta-ur-Rahman, Ed.; Elsevier: Amsterdam
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Danilov, L. L.; Shibaev, V. N. In Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 1991; Vol. 8, pp 63-114.
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Danilov, L.L.1
Shibaev, V.N.2
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22
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0000056380
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Lakowicz, J. R., Ed.; Plenum Press: New York
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Cheung, H. C. In Topics in Fluorescence Spectroscopy; Lakowicz, J. R., Ed.; Plenum Press: New York, 1991; Vol. 2, pp 127-176.
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Cheung, H.C.1
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