scholarly journals XXXVIII.—Intramolecular rearrangement in derivatives of the aromatic aminoketones

1904 ◽  
Vol 85 (0) ◽  
pp. 340-345 ◽  
Author(s):  
Frederick Daniel Chattaway
2014 ◽  
Vol 55 (30) ◽  
pp. 4193-4195 ◽  
Author(s):  
Jeffrey C. Pelletier ◽  
Venkata Velvadapu ◽  
Mark E. McDonnell ◽  
Jay E. Wrobel ◽  
Allen B. Reitz

ChemInform ◽  
2014 ◽  
Vol 45 (52) ◽  
pp. no-no
Author(s):  
Jeffrey C. Pelletier ◽  
Venkata Velvadapu ◽  
Mark E. McDonnell ◽  
Jay E. Wrobel ◽  
Allen B. Reitz

2002 ◽  
Vol 67 (12) ◽  
pp. 1805-1819 ◽  
Author(s):  
Jiří Kroutil ◽  
Jindřich Karban ◽  
Tomáš Trnka ◽  
Miloš Buděšínský ◽  
Miloslav Černý

The aziridine ring opening of N-tosylepimino carbohydrates 1-6 having D-allo, D-manno, D-galacto and D-talo configurations with benzyl alcohol, benzylamine and phenylmethanethiol afforded 2-, 3- and 4-O-benzyl-, benzylsulfanyl and benzylamino derivatives of 1,6-anhydro-β-D-hexopyranoses of D-gluco, D-galacto and D-manno configurations 7-23 in 44-99% yields. Hexenopyranoses 24-26 were prepared from tosylepimino carbohydrates 1, 4 and 5 by intramolecular rearrangement of the aziridine ring.


Sign in / Sign up

Export Citation Format

Share Document