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- Recent advancements in pharmacological strategies to modulate energy balance for combating obesity. Benudhara Pati, Satyabrata Sendh, Bijayashree Sahu, Sunil Pani, Nivedita Jena, Naresh Chandra Bal
, RSC Med. Chem.
, 2023
, 14
, 1429
- A carbene-catalyzed tandem isomerization/cyclisation strategy: an efficient assembly of benzoxazinones. Ming Lang, Jian Wang
, Org. Chem. Front.
, 2019
, 6
, 1367
- Current trends and future prospects of lipstatin: a lipase inhibitor and pro-drug for obesity. Punit Kumar, Kashyap Kumar Dubey
, RSC Adv.
, 2015
, 5
, 86954
- 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
- o-Acetoxylation of oxo-benzoxazines via C–H activation by palladium(ii)/aluminium oxide. Ramanand Prajapati, Ajay Kant Gola, Amrendra Kumar, Shubham Jaiswal, Narender Tadigoppula
, New J. Chem.
, 2022
, 46
, 5719
- TBHP-promoted multicomponent reaction to access 2-aminobenzoxazinones using sodium chlorodifluoroacetate as the C1 synthon. Huijuan Li, Yongfeng Wang, Cheng Xu, Jingwen Zou, Yaxuan Wu, Guodong Yin
, Org. Chem. Front.
, 2023
, 10
, 1988
- Ruthenium catalyzed chemo and site-selective C–H amidation of oxobenzoxazine derivatives with sulfonyl azides. Manickam Bakthadoss, Polu Vijay Kumar, Ravan Kumar, Manickam Surendar, Duddu S. Sharada
, New J. Chem.
, 2019
, 43
, 14190
- Difluorocarbene-enabled access to 1,3-oxazin-6-ones from enamides. Shuai Wang, Xin Li, Shengnan Jin, Kang Liu, Cong Dong, Jianke Su, Qiuling Song
, Org. Chem. Front.
, 2022
, 9
, 1282
- Palladium catalyzed chemo- and site-selective C–H acetoxylation and hydroxylation of oxobenzoxazine derivatives. Manickam Bakthadoss, Polu Vijay Kumar, Ravan Kumar, Vishal Agarwal
, Org. Biomol. Chem.
, 2019
, 17
, 4465
- Pd-Catalyzed regioselective C–H halogenation of quinazolinones and benzoxazinones. Minoo Dabiri, Noushin Farajinia Lehi, Siyavash Kazemi Movahed, Hamid Reza Khavasi
, Org. Biomol. Chem.
, 2017
, 15
, 6264