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4. (a) Merulinic acid: Giannetti, B. M.; Steglich, W.; Quack, W.; Anke, T.; Oberwinkler, F. Z. Naturforsch. 1978, 33C, 807-816. However, the stereochemistry at C-16 of the merulinic acids has not been unambiguously assigned.
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(b)For Suzuki-reactions with 9-alkyl-9-BBN derivatives see: Miyaura, N.; Ishiyama, T.; Sasaki, H.; Ishikawa, M.; Satoh, M.; Suzuki, A. J. Am. Chem. Soc. 1989, 111, 314-321.
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(e) Fürstner, A.; Seidel, G.; Gabor, B.; Kopiske, C.; Krüger, C.; Mynott, R. Tetrahedron 1995, 51, 8875-8888.
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(f)For an alternative concept see: Fürstner, A.; Seidel, G. Tetrahedron 1995, 51, 11165-11176.
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0011928302
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8. A Suzuki reaction of this triflate with an alkynylborate is the key-step in a recent synthesis of lunularic acid, c.f.: Fürstner, A.; Nikolakis, K., Liebigs Ann., 1996 (issue 12).
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0011927647
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No α-anomer could be detected in the NMR spectrum of crude 16; the manno:gluco ratio in the reduction step was > 10:1 (NMR, HPLC)
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13. No α-anomer could be detected in the NMR spectrum of crude 16; the manno:gluco ratio in the reduction step was > 10:1 (NMR, HPLC).
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38
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0000488020
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