ChemInform Abstract: Discovery and Application of Iminotriphenylphosphorane as a Formal Aromatic Primary Amine Protecting Group.

ChemInform ◽  
2013 ◽  
Vol 44 (3) ◽  
pp. no-no
Author(s):  
Benedicte Delouvrie ◽  
Herve Germain ◽  
Craig S. Harris ◽  
Maryannick Lamorlette ◽  
Honorine Lebraud ◽  
...  
2012 ◽  
Vol 53 (40) ◽  
pp. 5380-5384 ◽  
Author(s):  
Bénédicte Delouvrié ◽  
Hervé Germain ◽  
Craig S. Harris ◽  
Maryannick Lamorlette ◽  
Honorine Lebraud ◽  
...  

1981 ◽  
Vol 22 (19) ◽  
pp. 1787-1790 ◽  
Author(s):  
Stevan Djuric ◽  
John Venit ◽  
Philip Magnus

Author(s):  
Ankur A. Kaneria ◽  
Nilesh M. Thumar ◽  
Kartik D. Ladva ◽  
Milan S. Vadodaria

A convenient and promising synthesis of 4-(alkyl/aryl)- 3-(4-bromobenzyl)-5-(thiophen-2-yl)-4H-1,2,4-triazol was carried out by the reaction of 2-(4-bromobenzyl)-5-(thiophen-2-yl)-1,3,4-oxadiazole with different aliphatic/aromatic primary amine without any solvent. The newly synthesized compound were characterized by1H NMR, IR and Mass spectroscopy and also screened for their antimicrobial activity against various strains of bacteria and fungi.


Author(s):  
Sławomir Kasperowicz ◽  
Jolanta Czerwińska ◽  
Bartosz Majchrzak ◽  
Barbara Tudek ◽  
Adam Mieczkowski

5-Methyl-3,8-di-(2-amino-4-bromophenyl)-4,9-dioxa-1,2,6,7-tetraaza-5λ5-phosphaspiro[4.4]nona-2,7-diene was obtained in a condensation reaction of 2-amino-5-bromobenzohydrazide and methylphosphonyl dichloride in the presence of triethylamine. An initial biological screening was performed for the obtained product. The synthesized compound possesses two aromatic primary amine groups and two bromine atoms within the structure, which are suitable for further structural modifications.


2020 ◽  
Author(s):  
Rémi Blieck ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A dual copper/enamine catalytic system is found to enable an intermolecular enantioselective α-addition of various carbonyl nucleophiles to allenamides. Secondary amine catalysts allowed the highly enantioselective addition of aldehydes, while using primary amine catalysts led to the enantioselective addition of ketoester nucleophiles. The process was found to be highly regio-, stereo- and enantio-selective and represented the first allene hydrofunctionalization using an synergistic catalysis involving copper


Sign in / Sign up

Export Citation Format

Share Document