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- Proline-catalysed asymmetric amination of α,α-disubstituted aldehydes: synthesis of configurationally stable enantioenriched α-aminoaldehydes. Henning Vogt, Sylvia Vanderheiden, Stefan Bräse
, Chem. Commun.
, 2003
, 2448
- Inexpensive multigram-scale synthesis of cyclic enamines and 3-N spirocyclopropyl systems. Pratik Kumar, Omar Zainul, Scott T. Laughlin
, Org. Biomol. Chem.
, 2018
, 16
, 652
- 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
- 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
- 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
- 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
- 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
- Photocatalytic decarboxylative alkenylation of α-amino and α-hydroxy acid-derived redox active esters by NaI/PPh3 catalysis. Ya-Ting Wang, Ming-Chen Fu, Bin Zhao, Rui Shang, Yao Fu
, Chem. Commun.
, 2020
, 56
, 2495
- Recent advances in synthetic facets of immensely reactive azetidines. Vishu Mehra, Isha Lumb, Amit Anand, Vipan Kumar
, RSC Adv.
, 2017
, 7
, 45763