205372-01-6Relevant articles and documents
Studies directed towards the total synthesis of feigrisolide B
Sharma,Kumar, K. Raman
, p. 2323 - 2326 (2007/10/03)
Attempts directed towards the total synthesis of feigrisolide B resulted in the synthesis of lactones 1 and 2. The synthesis of 1 and 2 was achieved from d-glucose and l-malic acid, respectively, with a Ti(IV) mediated diastereoselective aldol reaction as
Studies on the stereochemistry of theonezolides A-C1: Elucidation of the relative configurations of 1,3-diol moieties of the C-4 ~ C-17 fragment
Kobayashi, Jun'ichi,Yonezawa, Makiko,Takeuchi, Shinji,Ishibashi, Masami
, p. 39 - 42 (2007/10/03)
Four model compounds having syn and anti 1,3-diol type moieties corresponding to C-8/C-10 and C-14/C-16 positions contained in the C-4 ~ C-17 fragment of theonezolides A-C were prepared. Comparison of their spectral data suggested that the 1,3-diol at C-8/C-10 and the OH/OMe groups at C-14/C-16 positions of theonezolides A-C were both syn.
A synthesis of a C1-C7 building block for the enantiomer of hennoxazole A utilizing a regioselective ring opening of a cyclic acetal
Shioiri, Takayuki,McFarlane, Nigel,Hamada, Yasumasa
, p. 73 - 76 (2007/10/03)
AC1-C7 building block (4) for the enantiomer of hennoxazole A(1), an antivirus and analgesic active marine natural product, was efficiently synthesized from (S)-malic acid utilizing the following key steps: (1) the stereoselective co