@article{98953b027e074ad5b9a5eb735d8bd5a4,
title = "The first total synthesis and structural determination of lagunamycin",
abstract = "Lagunamycin (1) has been synthesized by using our developed remote stereoinduction, Knorr condensation, periodinane oxidation, and diazonation. This enantioselective synthesis determined the absolute configuration of lagunamycin. Existence of rotational conformers was confirmed by NMR studies.",
author = "Seijiro Hosokawa and Shoichi Kuroda and Keisuke Imamura and Kuniaki Tatsuta",
note = "Funding Information: K.I. thanks to JSPS Research Fellowships for Young Scientists. The authors are grateful for financial support to 21 COE {\textquoteleft}Center for Practical Nano-Chemistry{\textquoteright}, Consolidated Research Institute for Advanced Science and Medical Care, and Grant-in-Aid for Scientific Research (A), Scientific Research (C), and Scientific Research on Priority Areas 16073220 from The Ministry of Education, Culture, Sports, Science and Technology (MEXT). ",
year = "2006",
month = aug,
day = "28",
doi = "10.1016/j.tetlet.2006.06.158",
language = "English",
volume = "47",
pages = "6183--6186",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "35",
}