@article{439f8f9bf1054a55993699b90d675066,
title = "Formal Synthesis of Pseudolaric Acid B",
abstract = "A formal synthesis of pseudolaric acid B, a diterpene isolated from the root bark of Pseudolarix kaempferi Gordon (Pinaceae), to Trost's synthetic intermediate was achieved in 17 steps from a known ketone. Key features of this synthesis include a Claisen rearrangement and iodoetherification to construct quaternary stereocenters and ring-closing metathesis to form the seven-membered ring.",
keywords = "Claisen rearrangement, cytotoxins, diterpenes, iodoetherification, pseudolaric acid B, total synthesis",
author = "Naoki Mori",
note = "Funding Information: This work was supported by Grant-in-Aid for Scientific Research (C) from the Japan Society for the Promotion of Science (Grant Number 16K07712).JapanSocietyforthePromotionofScience(16K07712) Publisher Copyright: {\textcopyright} 2020 Georg Thieme Verlag. All rights reserved.",
year = "2020",
month = jun,
day = "3",
doi = "10.1055/s-0039-1690829",
language = "English",
volume = "31",
pages = "907--910",
journal = "Synlett",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "9",
}