@article{48257305bacc4baf9ab1d99677c0b71c,
title = "Photomediated Spirocyclization of N-Benzyl Propiolamide with N-Iodosuccinimide for Access to Azaspiro[4.5]deca-6,9-diene-3,8-dione",
abstract = "A metal- and oxidant-free route for affording azaspiro[4.5]deca-6,9-diene-3,8-dione via photomediated iodinated spirocyclization of N-(4-methoxybenzyl) propiolamide has been developed. The reaction underwent a radical addition/ipso-cyclization/dearomatization process at room temperature and successfully constructed C-C and C-I bonds. This green and convenient approach could be generally expanded to produce a range of iodinated spirocyclization products in moderate to good yields.",
author = "Man Yang and Jiawei Hua and Hao Wang and Tao Ma and Chengkou Liu and Wei He and Ning Zhu and Yujing Hu and Zheng Fang and Kai Guo",
note = "Publisher Copyright: {\textcopyright} 2022 American Chemical Society. All rights reserved.",
year = "2022",
month = jul,
day = "1",
doi = "10.1021/acs.joc.2c00579",
language = "英语",
volume = "87",
pages = "8445--8457",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "13",
}