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Nicolaou, K.C.1
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c) K. C. Nicolaou, K. B. Simonsen, G. Vassilikogiannakis, P. S. Baran, V. P. Vidali, E. N. Pitsinos, E. A. Couladouros, Angew. Chem. 1999, 111, 3762;
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9
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0035932578
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a) A total synthesis of (+)-bisorbicillinol (2) in 51% ee has been reported, see: L. H. Pettus, R. W. Van de Water, T. R. R. Pettus, Org. Lett. 2001, 3, 905;
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10
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2542513317
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b) for a chiral-auxiliary-directed synthesis of chiral quinols bearing a heteroatom-substituted quaternary center, see: L. H. Mejorado, C. Hoarau, T. R. R. Pettus, Org. Lett. 2004, 6, 1535;
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1842587810
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c) for a comprehensive review, see: D. Magdziak, S. Meek, T. R. R. Pettus, Chem. Rev. 2004, 104, 1383.
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0000745211
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N. Nakajima, K. Horita, R. Abe, O. Yonemitsu, Tetrahedron Lett. 1988, 29, 4139.
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25
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20444395233
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note
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Alkynonyl ester 15 is prepared in quantitative yield from the reaction of commercially available ethyl malonyl chloride with 1-pentynylmagnesium chloride (see the Supporting Information).
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26
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0000540528
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a) D. Ma, Y. Lin, X. Lu, Y. Yu, Tetrahedron Lett. 1988, 29, 1045;
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Ma, D.1
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29
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0026608579
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for applications in syntheses, see: d) D. Desmaële, Tetrahedron 1992, 48, 2925;
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Desmaële, D.1
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32
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20444368192
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note
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[17b]: + 124.4° (c = 0.5, MeOH)).
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-
-
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33
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0000090699
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a) N. Abe, T. Murata, A. Hirota, Biosci. Biotechnol. Biochem. 1998, 62, 661;
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34
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0000553098
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b) N. Abe, T. Murata, A. Hirota, Biosci. Biotechnol. Biochem. 1998, 62, 2120.
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Hirota, A.3
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35
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20444378335
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note
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[7] consequently, the current asymmetric syntheses with (R)-9 as an intermediate provide direct experimental evidence confirming the previous assignment of the absolute configurations for (+)-2, (+)-4, and (+)-6 based on their biosynthesis hypothesis (see the Supporting Information).
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