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- Synthesis and biological evaluation of structurally diverse α-conformationally restricted chalcones and related analogues. Casey J. Maguire, Graham J. Carlson, Jacob W. Ford, Tracy E. Strecker, Ernest Hamel, Mary Lynn Trawick, Kevin G. Pinney
, Med. Chem. Commun.
, 2019
, 10
, 1445
- Autocatalytic deoximation reactions driven by visible light. Hongjia Li, Xiaobi Jing, Yaocheng Shi, Lei Yu
, React. Chem. Eng.
, 2021
, 6
, 119
- External-oxidant-free amino-benzoyloxylation of unactivated alkenes of unsaturated ketoximes with O-benzoylhydroxylamines. Jiangfei Chen, Yan-Ping Zhu, Jin-Heng Li, Qiu-An Wang
, Chem. Commun.
, 2021
, 57
, 5215
- Superelectrophilic activation of 1-nitronaphthalene in the presence of aluminum chloride. Reactions with benzene and cyclohexane. Zhongwei Zhu, Alexander M. Genaev, George E. Salnikov, Konstantin Yu. Koltunov
, Org. Biomol. Chem.
, 2018
, 16
, 9129
- Photocatalytic aerobic oxidative deoximation reaction with degradable rhodamine B. Feng Wang, Rongrong Qian, Lei Yu
, React. Chem. Eng.
, 2023
, 8
, 849
- Heteropolyacid catalyzed O-alkylation of oximes with alcohols via a carbocation in dimethyl carbonate and mechanism insight. Hongfeng Zhuang, Qin Hou, Feng Han, Haotian Lv, Chengxia Miao
, Green Chem.
, 2023
, 25
, 310
- Convenient synthesis of α-nitrooximes mediated by OXONE®. Napasawan Chumnanvej, Natthapol Samakkanad, Manat Pohmakotr, Vichai Reutrakul, Thaworn Jaipetch, Darunee Soorukram, Chutima Kuhakarn
, RSC Adv.
, 2014
, 4
, 59726
- Chasing the agostic interaction in ligand assisted cyclometallation reactions of palladium(ii) . M. Arif Sajjad, Kirsten E. Christensen, Nicholas H. Rees, Peter Schwerdtfeger, John A. Harrison, Alastair J. Nielson
, Dalton Trans.
, 2017
, 46
, 16126
- Revisiting secondary interactions in neighboring group participation, exemplified by reactivity changes of iminylium intermediates. Yingtang Ning, Tomoya Fukuda, Hirotaka Ikeda, Yuko Otani, Masatoshi Kawahata, Kentaro Yamaguchi, Tomohiko Ohwada
, Org. Biomol. Chem.
, 2017
, 15
, 1381
- New complexity for aromatic ring agostic interactions. M. Arif Sajjad, Kirsten E. Christensen, Nicholas H. Rees, Peter Schwerdtfeger, John A. Harrison, Alastair J. Nielson
, Chem. Commun.
, 2017
, 53
, 4187