The C11-C22 and C23-C35 segments 2 and 3 of reidispongiolide A (1), an actin-depolymerizing marine macrolide, were synthesized enantioselectively in 12 steps from (R)-glycidyl trityl ether and in 12 steps from chiral ketone 15, respectively.
โฆ LIBER โฆ
Synthetic study of marine macrolide swinholide A. stereocontrolled synthesis of the C11 - C23 segment
โ Scribed by Tadashi Nakata; Toshiya Komatsu; Kazuo Nagasawa; Haruo Yamada; Takashi Takahashi
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 336 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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