Synthesis of Oxazolidin-2-ones and Imidazolidin-2-ones Directly from 1,3-Diols or 3-Amino Alcohols using Iodobenzene Dichloride and Sodium Azide

2014 ◽  
Vol 356 (5) ◽  
pp. 1113-1118 ◽  
Author(s):  
Tian He ◽  
Wen-Chao Gao ◽  
Wei-Kun Wang ◽  
Chi Zhang
Keyword(s):  
Sodium Azide ◽  
Amino Alcohols

ChemInform Abstract: Synthesis of Enantiopure 1,2-Azido and 1,2-Amino Alcohols via Regio- and Stereoselective Ring-Opening of Enantiopure Epoxides by Sodium Azide in Hot Water.

ChemInform ◽  
2016 ◽  
Vol 47 (24) ◽  
Author(s):  
Hai-Yang Wang ◽  
Kun Huang ◽  
Melvin De Jesus ◽  
Sandraliz Espinosa ◽  
Luis E. Pinero-Santiago ◽  
...  
Keyword(s):  
Sodium Azide ◽  
Ring Opening ◽  
Amino Alcohols ◽  
Hot Water ◽  
Enantiopure Epoxides

scholarly journals Synthesis of enantiopure 1,2-azido and 1,2-amino alcohols via regio- and stereoselective ring-opening of enantiopure epoxides by sodium azide in hot water

2016 ◽  
Vol 27 (2-3) ◽  
pp. 91-100 ◽  
Author(s):  
Hai-Yang Wang ◽  
Kun Huang ◽  
Melvin De Jesús ◽  
Sandraliz Espinosa ◽  
Luis E. Piñero-Santiago ◽  
...  
Keyword(s):  
Sodium Azide ◽  
Ring Opening ◽  
Amino Alcohols ◽  
Hot Water ◽  
Enantiopure Epoxides

Tetrazoloquinolines: Synthesis, Reactions, and Applications

2020 ◽  
Vol 24 (4) ◽  
pp. 439-464 ◽  
Author(s):  
Rizk E. Khidre ◽  
Tahah A. Ameen ◽  
Mounir A. I. Salem
Keyword(s):  
Carboxylic Acid ◽  
Chemical Reactions ◽  
Sodium Azide ◽  
Biological Activities ◽  
Quinoline Derivatives ◽  
Pharmacological Activities ◽  
Synthesis Reactions ◽  
Intramolecular Cyclocondensation

This review summarizes the synthesis, reactions, and biological activities of tetrazolo[1,5-a]quinoline derivatives. These derivatives were synthesized by several methods such as i) from the reaction of 2-chloroquinoline with sodium azide ii) from diazotization 2-hydrazinylquinoline derivatives, and iii) from intramolecular cyclocondensation of 2-azidoarylidenes. Also, the chemical reactions and pharmacological activities of some tetrazoloquinolines such as tetrazolo[1,5-a]quinoline-4-carbaldehyde, 5-chlorotetrazolo[ 1,5-a]quinoline, 4-(chloromethyl)tetrazolo[1,5-a]quinoline, tetrazolo[1,5- a]quinoline-4-carboxylic acid, and 5-azidotetrazolo[1,5-a]quinoline were discussed.

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