@article{3084cf54db4e404ea02151bb9234ee31,
title = "Synthetic studies on thiostrepton family of peptide antibiotics: Synthesis of the cyclic core portion containing the dehydropiperidine, dihydroquinoline, L-valine, and masked dehydroalanine segments",
abstract = "The cyclic core portion containing the dehydropiperidine, dihydroquinoline, L-valine, and masked dehydroalanine (i.e., β-phenylselenoalanine) segments of the thiostrepton family of peptide antibiotics was synthesized via the consecutive coupling of these four segments followed by cyclization at the amide bond between the dehydropiperidine and masked dehydroalanine segments.",
keywords = "Dehydroalanine, Dehydropiperidine, Dihydroquinoline, Thiostrepton, Ytterbium triflate",
author = "Tomonori Mori and Hiraku Tohmiya and Yukiko Satouchi and Shuhei Higashibayashi and Kimiko Hashimoto and Masaya Nakata",
note = "Funding Information: We thank Professor Shuichi Matsumura (Keio University) for the measurement of the mass spectrum of 2 . This research was partially supported by a Grant-in-Aid for the 21st Century COE program {\textquoteleft}KEIO Life Conjugate Chemistry{\textquoteright} from the Ministry of Education, Culture, Sports, Science, and Technology, Japan, and a Grant-in-Aid for Scientific Research on Priority Areas (A) {\textquoteleft}Exploitation of Multi-Element Cyclic Molecules{\textquoteright} from the Ministry of Education, Culture, Sports, Science, and Technology, Japan.",
year = "2005",
month = sep,
day = "19",
doi = "10.1016/j.tetlet.2005.07.122",
language = "English",
volume = "46",
pages = "6423--6427",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "38",
}