Abstract

AbstractProgress on a stereocontrolled total synthesis of the pseudo aglycone of apoptolidin (2) starting from (S)‐epichlorohydrin is reported. The lower C(12)–C(28) fragment (4) was derived by consecutive stereoselective aldol reactions and extended using a Suzuki cross‐coupling reaction. Studies on glycoyslation of the C9 hydroxy group are also described. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)

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