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72849114062
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Compound 11 was prepared following a similar literature procedure, see: C.R. Reddy, G. Dharmapuri, and N.N. Rao Org. Lett. 11 2009 5730 5733
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28
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79952537355
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Asymmetric dihydroxylation of 11 was similar to the synthesis of ent-11 as reported in the above reference
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Asymmetric dihydroxylation of 11 was similar to the synthesis of ent-11 as reported in the above reference.
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29
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20444490799
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For similar regio- and stereoselective asymmetric dihydroxylation of distant olefinic bond of a α,β,γ,δ-unsaturated esters see: Y. Zhang, and G.A. O'Doherty Tetrahedron 61 2005 6337 6351
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(2005)
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Zhang, Y.1
O'Doherty, G.A.2
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33
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79952534446
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+: 311.2222, found: 311.2225.
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+: 311.2222, found: 311.2225.
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-
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34
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79952533648
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+: 427.2824, found: 427.2831.
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+: 427.2824, found: 427.2831.
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-
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35
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79952536767
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For a similar low yielding RCM reaction in the synthesis of helicholactone using Grubbs-II catalyst see Ref. 4a
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For a similar low yielding RCM reaction in the synthesis of helicholactone using Grubbs-II catalyst see Ref. 4a.
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36
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79952534640
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4 (in the synthesis of halicholactone) see Refs. 4a and 4d
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4 (in the synthesis of halicholactone) see Refs. 4a and 4d.
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37
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79952534758
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+: 359.2356, found: 359.2350
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+: 359.2356, found: 359.2350.
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