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- Synthesis of medium-sized heterocycles from oxetanes based on an allylic amination/ring-opening strategy. Jixing Li, Ming Fang, Maoyan Liao, Hongling Xie, Xiu-Qin Dong, Zhengyu Han, Jianwei Sun, Hai Huang
, Chem. Commun.
, 2023
, 59
, 14467
- Strain-release enabled [3 + 2] annulation of 3-aminooxetanes with simple CN bonds: facile synthesis of imidazolidines. Jing Zhang, Yi-Fei Li, Feng-Cheng Jia, Yang Gao, Xiao-Qiang Hu
, Org. Chem. Front.
, 2021
, 8
, 6616
- Synthesis and structure of oxetane containing tripeptide motifs. Nicola H. Powell, Guy J. Clarkson, Rebecca Notman, Piotr Raubo, Nathaniel G. Martin, Michael Shipman
, Chem. Commun.
, 2014
, 50
, 8797
- Recent advances in the tandem copper-catalyzed Ullmann–Goldberg N-arylation–cyclization strategies. Jyoti M. Honnanayakanavar, Owk Obulesu, Surisetti Suresh
, Org. Biomol. Chem.
, 2022
, 20
, 2993
- A multicomponent reaction of isocyanides, selenium powder and 3-aminooxetanes in pure water: green and efficient synthesis of 1,3-selenazolines. Huan Liu, Zi-Lin Ye, Zhong-Jian Cai, Shun-Jun Ji
, Green Chem.
, 2023
, 25
, 4239
- 3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions. Zengwei Lai, Renwei Zhang, Qiang Feng, Jianwei Sun
, Chem. Sci.
, 2020
, 11
, 9945
- A mild catalytic synthesis of 2-oxazolines via oxetane ring-opening: rapid access to a diverse family of natural products. Hai Huang, Wen Yang, Zuliang Chen, Zengwei Lai, Jianwei Sun
, Chem. Sci.
, 2019
, 10
, 9586
- Stereospecific conversion of (1R*,3S*)- and (1R*,3R*)-3-cyclohexyl-1-phenylpropane-1,3-diol into the corresponding 2,4-disubstituted oxetanes. Tajassus Aftab, Christabel Carter, Martin Christlieb, Jennifer Hart, Adam Nelson
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 711
- N–H⋯X interactions stabilize intra-residue C5 hydrogen bonded conformations in heterocyclic α-amino acid derivatives. Venkateswara Rao Mundlapati, Zeynab Imani, Viola C. D'mello, Valérie Brenner, Eric Gloaguen, Jean-Pierre Baltaze, Sylvie Robin, Michel Mons, David J. Aitken
, Chem. Sci.
, 2021
, 12
, 14826