@article{c65b0874ad3042dbbabaf6a23a3a770d,
title = "The efficient entry into the tricyclic core of halichlorine",
abstract = "An efficient and diastereoselective synthesis of the tricyclic core structure 3 found in the marine alkaloid halichlorine 1 has been accomplished starting from Grigg's tricyclic isoxazolidine 5, which was prepared by the tandem intramolecular Michael addition-[3+2] cycloaddition of the corresponding oxime of 4. (C) 2000 Elsevier Science Ltd.",
author = "Mitsuru Shindo and Fukuda, {Yu Ichi} and Kozo Shishido",
note = "Funding Information: This work was supported by a Grant-in-Aid for Scientific Research (No. 11557172) from the Ministry of Education, Science, Sports and Culture, Japan, Uehara Memorial Foundation (M.S.), and Takeda Science Foundation (M.S.). We are grateful to Professor Tetsuto Tsunoda and Mr. Hiroto Kaku, Tokushima Bunri University, for valuable discussions and technical assistance. We also thank Mr. Masahiko Bando, Otsuka Pharmaceutical Co. Ltd, for the X-ray analysis. Copyright: Copyright 2004 Elsevier Science B.V., Amsterdam. All rights reserved.",
year = "2000",
month = feb,
day = "5",
doi = "10.1016/S0040-4039(99)02192-9",
language = "English",
volume = "41",
pages = "929--932",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "6",
}
