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- Photoredox catalyzed cascade CF3 addition/chemodivergent annulations of ortho-alkenyl aryl ureas. Sakamuri Sarath Babu, A Anagha Varma, Purushothaman Gopinath
, Chem. Commun.
, 2022
, 58
, 1990
- Catalyst-free 1 : 2 annulation of quinolines with trifluoroacetylacetylenes: an access to functionalized oxazinoquinolines. K. V. Belyaeva, L. P. Nikitina, A. V. Afonin, A. V. Vashchenko, V. M. Muzalevskiy, V. G. Nenajdenko, B. A. Trofimov
, Org. Biomol. Chem.
, 2018
, 16
, 8038
- Diastereoselective synthesis of CF3-oxazinoquinolines in water. Vasiliy M. Muzalevskiy, Kseniya V. Belyaeva, Boris A. Trofimov, Valentine G. Nenajdenko
, Green Chem.
, 2019
, 21
, 6353
- Palladium-catalyzed asymmetric [4+2] annulation of vinyl benzoxazinanones with pyrazolone 4,5-diones to access spirobenzoxazine frameworks. Ben-Hong Chen, Shuai-Jiang Liu, Qian Zhao, Qiumeng Hou, Jia-Li Yuan, Gu Zhan, Qian-Qian Yang, Wei Huang
, Chem. Commun.
, 2023
, 59
, 1233
- Synthesis of benzo[1,3]oxazines via copper(i)-catalyzed cascade annulation of nitriles, aldehydes and diaryliodonium salts. Jinyu Sheng, Xiang Su, Chengyao Cao, Chao Chen
, Org. Chem. Front.
, 2016
, 3
, 501
- Intramolecular C–O/C–S bond insertion of α-diazoesters for the synthesis of 2-aryl-4H-benzo[d][1,3]oxazine and 2-aryl-4H-benzo[d][1,3]thiazine derivatives. B. V. Subba Reddy, R. Anji Babu, M. Ramana Reddy, B. Jagan Mohan Reddy, B. Sridhar
, RSC Adv.
, 2014
, 4
, 44629
- Base-mediated [2 + 4] cycloadditions of in situ formed azaoxyallyl cations with N-(2-chloromethyl)aryl amides. Qiaomei Jin, Meng Gao, Dongjian Zhang, Cuihua Jiang, Nan Yao, Jian Zhang
, Org. Biomol. Chem.
, 2018
, 16
, 7336
- Palladium-catalyzed synthesis of 4-sila-4H-benzo[d][1,3]oxazines by intramolecular Hiyama coupling. Donghyeon Lee, Ryo Shintani
, Chem. Sci.
, 2023
, 14
, 4114
- Catalytic enantioselective oxysulfenylation of o-vinylanilides. Arunachalam Kesavan, Pazhamalai Anbarasan
, Chem. Commun.
, 2022
, 58
, 282
- Fluorination methods in drug discovery. Damian E. Yerien, Sergio Bonesi, Al Postigo
, Org. Biomol. Chem.
, 2016
, 14
, 8398