75825-04-6Relevant articles and documents
A FACILE THREE-STEP SYNTHESIS OF A RACEMIC 4,5-DIAMINO-4,5-DIDEOXY-α-D,β-L-LYXOPYRANOSE.
Streith, Jacques,Augelmann, Gerard,Fritz, Hans,Strub, Henri
, p. 1909 - 1912 (1982)
Diels-Alder cycloaddition of nitrosobenzene to 1-methoxycarbonyl-1,2-dihydropyridine led in high yield to the endocyclic hydroxylamine adduct 5.which was successively oxydized with potassium permanganate and hydrogenolyzed to give the new aminosugar 4,5-d
Diels-Alder cycloadditions of N-substituted-1,2-dihydropyridines with nitrosobenzene. Synthesis of 3-phenyl-2-oxa-3,6-diazabicyclooct-7-enes
Knaus, Edward E.,Avasthi, Kamlakar,Giam, C. S.
, p. 2447 - 2451 (2007/10/02)
The regiospecific (?2 + ?4) cycloaddition reaction of N-carbonyl-1,2-dihydropyridines 2 with nitrosobenzene afford a mixture of 3-phenyl-2-oxa-3,6-diazabicyclooct-7-ene rotamers 3 and 4.Rotamers 3 and 4, which differ in configuration at the carbony