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Ceroplasteric acid

Rigby et al. employed the Ireland-Claisen rearrangement in an approacdi to the ophiobolane ceroplasteric acid (Scheme4.118) [114]. The product was isolated as a 4 1 mixture of diastereomers at C2 (pentenoic acid numbering). The major product is consistent with rearrangement occurring via a chair transition state for an -silyl ketene acetal or a boat transition state for a Z-sUyl ketene acetal. [Pg.186]

Ceroplasteric acid, T41 Ceroplastol I, T41 Cervicarcin, Y18 Cevine, K35 Chaenorhine, KIO ... [Pg.159]

See other pages where Ceroplasteric acid is mentioned: [Pg.456]    [Pg.457]    [Pg.457]    [Pg.458]    [Pg.462]    [Pg.186]    [Pg.186]    [Pg.118]    [Pg.302]    [Pg.107]    [Pg.107]    [Pg.456]    [Pg.457]    [Pg.457]    [Pg.458]    [Pg.462]    [Pg.186]    [Pg.186]    [Pg.118]    [Pg.302]    [Pg.107]    [Pg.107]   
See also in sourсe #XX -- [ Pg.563 ]

See also in sourсe #XX -- [ Pg.563 ]

See also in sourсe #XX -- [ Pg.41 ]

See also in sourсe #XX -- [ Pg.186 ]

See also in sourсe #XX -- [ Pg.4 , Pg.7 , Pg.107 ]



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