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Volumn 121, Issue 13, 1999, Pages 3072-3082

Enantioselective total synthesis of (+)-taxusin

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL; CYCLOPROPANE DERIVATIVE; DITERPENE; KETONE; METHANOL; TAXANE DERIVATIVE;

EID: 0033531680     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja984250f     Document Type: Article
Times cited : (42)

References (55)
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    • note
    • The taxane numbering system, as illustrated in Figure 1, is used throughout.
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    • note
    • 13 and confirmed by the completion of the total synthesis of (+)-taxusin.
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    • The relative stereochemistry was inferred from the analogy of a closely related compound, the stereochemistry of which was confirmed by the X-ray analysis of its derivative, see: Takenaka, Y.; Sakai, Y.; Ohashi, Y.; Furukawa, T.; Horiguchi, Y.; Kuwajima, I. Anal. Sci. 1993, 9, 883.
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    • note
    • Although the cyclization precursor 13 consisted of Z configuration at the benzyl enol ether moiety exclusively, E/Z isomerization took place under the cyclization reaction conditions and the thermodynamically most stable tricarbocycle 14 with the C10β substituent was obtained as a major product. For the proposed mechanism of the E/Z isomerization; see, ref 10d.
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    • note
    • iPr) gave considerable amounts of aldehydes (>50%) along with a small amount of 14 (ca. 30%).
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    • For angular methyl group introduction via reductive cleavage of cyclopropyl ketones, see: Dauben, W. G.; Deviny; E. J. J. Org. Chem. 1966, 31, 3794.
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    • SPARTAN ver. 4.1 (PM3) and MacroModel ver. 6.0 (MM2) were used for calculation
    • SPARTAN ver. 4.1 (PM3) and MacroModel ver. 6.0 (MM2) were used for calculation.


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