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Ohno, M.; Mori, K.; Hattori, T.; Eguchi, S. J. Org. Chem. 1990, 55, 6086-6091.
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79953174336
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note
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1H NMR spectrum, the α-methylene protons of the formyl group exhibit significant difference between their chemical shifts, with Δδ being 0.50 ppm for ent-6 and 0.53 ppm for 10. For exo products, the corresponding Δδ values are below 0.20 ppm (mostly below 0.10 ppm). See Ref. 8 and Ref. 10.
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26
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0242467669
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For structurally closely related natural products
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For structurally closely related natural products: (a) Sutthivaiyakit, S.; Nakorn, N. N.; Kraus, W.; Sutthivaiyakit, P. Tetrahedron 2003, 59, 9991-9995;
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Sutthivaiyakit, S.1
Nakorn, N.N.2
Kraus, W.3
Sutthivaiyakit, P.4
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0043022024
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(b) Peng, G.-P.; Tian, G.; Huang, X. -F.; Lou, F.-C. Phytochemistry 2003, 63, 877-881;
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Peng, G.-P.1
Tian, G.2
Huang, X.F.3
Lou, F.-C.4
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28
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45649084741
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(c) Wang, H.-X.; Liu, C.-M.; Liu, Q.; Gao, K. Phytochemistry 2008, 69, 2088-2094;
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Wang, H.-X.1
Liu, C.-M.2
Liu, Q.3
Gao, K.4
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29
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0034824177
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For a possible application in phorbol synthesis, see
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For a possible application in phorbol synthesis, see: Lee, K.; Cha, J. K. J. Am. Chem. Soc. 2001, 123, 5590-5591.
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J. Am. Chem. Soc.
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Lee, K.1
Cha, J.K.2
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79953168856
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note
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Similar situation was also encountered in Ref. 5.
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31
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79953207749
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note
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A structurally closely related compound (7 in Ref. 5) has been utilized for the formal synthesis of englerin A. See Ref. 5.
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32
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79953175676
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note
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The mixture of 10a/10b underwent the identical protocol depicted in Scheme 3 to deliver regioisomers in the same yield.
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