@article{35f295c252ff43ea8d5958e9b034fea3,
title = "Total synthesis and stereochemical reassignment of maedamide",
abstract = "Abstract The first total synthesis of maedamide, an acyclic peptide isolated from a marine cyanobacterial assemblage of Lyngbya sp., was achieved. This synthesis led to reassignment of the allo-d-Ile of maedamide to be l-Ile, which was supported by 1H and 13C NMR data.",
keywords = "Lyngbya, Maedamide, Marine cyanobacteria, Marine natural products, Total synthesis",
author = "Ayano Takayanagi and Arihiro Iwasaki and Kiyotake Suenaga",
note = "Funding Information: This work was supported in part by a Grants-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan ( 24310160 ) and Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research. Publisher Copyright: {\textcopyright} 2015 Elsevier Ltd.",
year = "2015",
month = jul,
day = "20",
doi = "10.1016/j.tetlet.2015.06.090",
language = "English",
volume = "56",
pages = "4947--4949",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "34",
}
