@article{6cd8b7e2abe14f49a30e6f726fb373d2,
title = "Concise total synthesis of acortatarin A",
abstract = "The spirocyclic pyrrole alkaloid, acortatarin A, which had been isolated from a Chinese medicinal plant, was synthesized from a known olefinic compound by a concise six-step sequence involving N-alkylation of a pyrrole derivative with an α-bromo ketone intermediate as the key step.",
keywords = "Acortatarin, N-alkylation, Reactive oxygen species, Spiro acetal",
author = "Takaaki Teranishi and Masayuki Kageyama and Shigefumi Kuwahara",
note = "Funding Information: This work was supported, in part, by grant-aid for scientific research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (no. 22380064).",
year = "2013",
doi = "10.1271/bbb.120862",
language = "English",
volume = "77",
pages = "676--678",
journal = "Bioscience, Biotechnology and Biochemistry",
issn = "0916-8451",
publisher = "Japan Society for Bioscience Biotechnology and Agrochemistry",
number = "3",
}