@article{b89481ddbc1d4eb9b4e087d6a9010c43,
title = "Total synthesis of (-)-Haouamine B pentaacetate and structural revision of haouamine B",
abstract = "The enantiocontrolled total synthesis of (-)-haouamine B pentaacetate was accomplished via an optically active indane-fused β-lactam, which was prepared by a newly developed Friedel-Crafts reaction. Subsequent cleavage of the β-lactam and an intramolecular McMurry coupling reaction provided the core indane-fused tetrahydropyridine, which led to the elucidation of the structure, as proposed by Trauner and Zub{\'i}a.",
keywords = "Alkaloids, Aromatic substitution, Cross-coupling, Cyclization, Total synthesis",
author = "Yuichi Momoi and Okuyama, {Kei Ichiro} and Hiroki Toya and Kenji Sugimoto and Kentaro Okano and Hidetoshi Tokuyama",
note = "Publisher Copyright: {\textcopyright} 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.",
year = "2014",
month = nov,
day = "24",
doi = "10.1002/anie.201407686",
language = "英語",
volume = "53",
pages = "13215--13219",
journal = "Angewandte Chemie - International Edition",
issn = "1433-7851",
publisher = "John Wiley and Sons Ltd",
number = "48",
}