- Microwave-Assisted Suzuki-Miyaura Cross Coupling using Nickel as Catalyst to Rapidly Access to 3-ArylazetidineBy Dequirez, Geoffroy et al, ChemistrySelect, 2017, 2(28), 8841-8846
Cas no 2222044-40-6 (1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester)
2222044-40-6 structure
Product Name:1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester
CAS No:2222044-40-6
MF:C17H32N2O3
MW:312.447585105896
CID:5577520
Update Time:2023-08-22
1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester Chemical and Physical Properties
Names and Identifiers
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- 1,1-Dimethylethyl 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-1-azetidinecarboxylate
- 1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester
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- Inchi: 1S/C17H32N2O3/c1-15(2,3)21-14(20)18-11-13(12-18)22-19-16(4,5)9-8-10-17(19,6)7/h13H,8-12H2,1-7H3
- InChI Key: NWGPNWXGHNUKSO-UHFFFAOYSA-N
- SMILES: C(OC(C)(C)C)(N1CC(C1)ON1C(CCCC1(C)C)(C)C)=O
1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester Production Method
Production Method 1
Reaction Conditions
1.1R:(Me3Si)2NH ?Na, C:13462-90-3, C:5456-63-3, S:Me2CHOH, S:THF, 30 min, 80°C
Reference
1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester Raw materials
1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester Preparation Products
1-Azetidinecarboxylic acid, 3-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, 1,1-dimethylethyl ester Related Literature
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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