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Regiospecific synthesis of neuroprotective 1,4-benzoxazine derivatives through a tandem oxidation–Diels–Alder reaction . Khac Minh Huy Nguyen, Leslie Schwendimann, Pierre Gressens, Martine Largeron
, Org. Biomol. Chem.
, 2015
, 13
, 3749
Some single electron-transfer reactions of arylimines
. David W. Brown, Monika Lindquist, Mary F. Mahon, Bengt Malm, Göran N. Nilsson, Aleyamma Ninan, Malcolm Sainsbury, Christer Westerlund
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2337
716. 3,4-Dihydro-2H -1,4-benzoxazines . J. Hill, G. R. Ramage
, J. Chem. Soc.
, 1964
, 3709
A transition-metal-free multicomponent reaction towards constructing chiral 2H -1,4-benzoxazine scaffolds . Lixiang Zhu, Xiaoyu Ren, Juan Du, Jia-Hong Wu, Jian-Ping Tan, Jixing Che, Jianke Pan, Tianli Wang
, Green Chem.
, 2020
, 22
, 7506
Total synthesis of heptacyclic Aspidosperma alkaloids. Part 1. Preliminary experiments . John W. Blowers, James P. Brennan, J. Edwin Saxton
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 2079
Dual SN Ar reaction in activated ortho -halonitrobenzene: direct synthesis of substituted 1,2,3,4-tetrahydroquinoxalines, 2,3-dihydro-1,4-benzoxazines, and 1,4-benzodioxines . Mahesh S. Deshmukh, Biswajit Das, Nidhi Jain
, RSC Adv.
, 2013
, 3
, 22389
Total synthesis of heptacyclic Aspidosperma alkaloids. Part 3. Synthesis of an advanced intermediate in the synthesis of alalakine . Abdelhamid Belattar, J. Edwin Saxton
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 679
Asymmetric hydrogenation of 3-substituted 2H -1,4-benzoxazines with chiral cationic Ru-MsDPEN catalysts: a remarkable counteranion effect . Jie Qin, Fei Chen, Yan-Mei He, Qing-Hua Fan
, Org. Chem. Front.
, 2014
, 1
, 952
Base-mediated intramolecular one-pot double-cyclization of epoxide-tethered 2-fluorobenzenesulfonamides: an avenue to 1,4-benzoxazine-fused benzothiaoxazepine-1,1-dioxides . Jonali Das, Biraj Jyoti Borah, Sajal Kumar Das
, Org. Biomol. Chem.
, 2020
, 18
, 220
A metal-free hydrogenation of 3-substituted 2H -1,4-benzoxazines . Simin Wei, Xiangqing Feng, Haifeng Du
, Org. Biomol. Chem.
, 2016
, 14
, 8026