@article{9cf007ee7f6141f9a848e71a226f85ca,
title = "Synthetic studies on reidispongiolide A, an actin-depolymerizing marine macrolide: synthesis of C11-C22 and C23-C35 segments",
abstract = "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.",
author = "Satoshi Akiyama and Eisuke Toriihara and Kazushi Suzuki and Toshiaki Teruya and Kiyotake Suenaga",
note = "Funding Information: This work was supported in part by Keio Gijuku Academic Development Funds, the Naito Foundation, and the Asahi Glass Foundation. We are grateful to Daiso Co., Ltd for the donation of chiral glycidyl trityl ether. We thank Kaneka Corporation for their gift of chiral methyl 3-hydroxy-2-methylpropionate.",
year = "2009",
month = sep,
day = "2",
doi = "10.1016/j.tetlet.2009.06.075",
language = "English",
volume = "50",
pages = "5012--5014",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "35",
}
