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- Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro-N-sulfinylimines. Gert Callebaut, Sven Mangelinckx, Loránd Kiss, Reijo Sillanpää, Ferenc Fülöp, Norbert De Kimpe
, Org. Biomol. Chem.
, 2012
, 10
, 2326
- Correlation between metal complex formation and biological activity of nicotianamine analogues. Giorgio Anderegg, Helmut Ripperger
, J. Chem. Soc., Chem. Commun.
, 1989
, 647
- The microwave-assisted syntheses and applications of non-fused single-nitrogen-containing heterocycles. Jay Prakash Soni, Krishna Sowjanya Chemitikanti, Swanand Vinayak Joshi, Nagula Shankaraiah
, Org. Biomol. Chem.
, 2020
, 18
, 9737
- Catalysts’ evolution in the asymmetric conjugate addition of nitroalkanes to electron-poor alkenes. Roberto Ballini, Alessandro Palmieri, Marino Petrini
, Org. Chem. Front.
, 2022
, 9
, 6077
- Sequential polypeptides. Part VI. The synthesis of some sequential polypeptide collagen models containing proline analogues. R. Fairweather, J. H. Jones
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2475
- Synthesis of poly-(L-azetidine-2-carboxylic acid). Renzo Boni, Antonio S. Verdini
, J. Chem. Soc., Perkin Trans. 1
, 1974
, 2173
- Base-promoted diastereoselective α-alkylation of borane N-((S)-1′-phenylethyl)azetidine-2-carboxylic acid ester complexes. Eiji Tayama, Ryotaro Nishio, Yoshiaki Kobayashi
, Org. Biomol. Chem.
, 2018
, 16
, 5833
- Synthesis of optically active 2-substituted azetidine-2-carbonitriles from chiral 1-arylethylamine via α-alkylation of N-borane complexes. Eiji Tayama, Nobuhiro Nakanome
, RSC Adv.
, 2021
, 11
, 23825
- Structural and mechanistic studies of the base-induced Sommelet–Hauser rearrangement of N-α-branched benzylic azetidine-2-carboxylic acid-derived ammonium salts. Eiji Tayama, Kazutoshi Watanabe, Sho Sotome
, Org. Biomol. Chem.
, 2017
, 15
, 6668
- Biosyntheses of azetidine-containing natural products. Linlin Pang, Daichen Yao, Fenghui Gao, Xiaoying Bian, Youming Zhang, Guannan Zhong
, Org. Biomol. Chem.
, 2023
, 21
, 7242