@article{7cc8b272047d410fa3b389e82f13b299,
title = "Toward the Synthesis of Yuzurimine-Type Alkaloids: Stereoselective Construction of the Heterocyclic Portions of Deoxyyuzurimine and Macrodaphnine",
abstract = "The heterocyclic portions of yuzurimine-type alkaloids, such as deoxyyuzurimine and macrodaphnine, were synthesized by using a stereoselective hydroboration-oxidation reaction to install the C20 methyl group, the intramolecular Mitsunobu reaction to construct the E-ring portion, and the intramolecular SN2 reaction to construct the F-ring portion as key steps.",
author = "Ichiro Hayakawa and Ryosuke Nagatani and Masaki Ikeda and Yoo, {Dong Eun} and Keita Saito and Hideo Kigoshi and Akira Sakakura",
note = "Funding Information: This work was supported by a Grant-in-Aid for Scientific Research (Grant Number 25350960) from the Japanese Society for the Promotion of Science (JSPS)/the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan; by a grant from the Kurata Grant awarded by the Kurata Memorial Hitachi Science and Technology; and by a grant from the NOVARTIS Foundation (Japan) for the Promotion of Science. The authors thank the Division of Instrumental Analysis, Okayama University for the NMR and HR-ESIMS measurements. Publisher Copyright: {\textcopyright} 2019 American Chemical Society.",
year = "2019",
month = aug,
day = "16",
doi = "10.1021/acs.orglett.9b02232",
language = "English",
volume = "21",
pages = "6337--6341",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "16",
}