108155-64-2Relevant academic research and scientific papers
SURPRISING REACTIONS OF SPECIAL AZOOLEFINS - SELF-ARYLATION, INDOLE RING CLOSURE, MILD CHLORINE SUBSTITUTION, AND "TERT. AMINO EFFECT"
Kirschke, K.,Moeller, A.,Schmitz, E.,Kuban, R. J.,Schulz, B.
, p. 4281 - 4284 (2007/10/02)
Azoolefins 2 either decompose or react with aryldiimines with uptake of an aryl group to give compounds 3.The latter can undergo ring closure to N-amino-indoles 4.In the 2,4,6-trichloro compound 3b orthochlorines are selectively replaced by morpholine under very mild conditions giving 5a, which easily fragments to form the benzimidazole 7.
SYNTHESIS OF THE TETRASACCHARIDE REPEATING UNIT OF THE O-SPECIFIC POLYSACCHARIDE FROM SALMONELLA MUENSTER AND SALMONELLA MINEAPOLIS
Kochetkov, N. K.,Torgov, V. I.,Malysheva, N. N.,Shashkov, A. S.,Klimov, E. M.
, p. 1227 - 1230 (2007/10/02)
The tetrasaccharide β-D-Man-(1-->4)-α-L-Rha-(1-->3)-D-Gal-(4--1)-α-D-Glc the repeating unit of the O-specific polysaccharide chain of the lipopolysaccharides from Salmonella muenster and S. mineapolis was obtained by glycosylation of benzyl 2,6-di-O-benz
