26396-67-8Relevant academic research and scientific papers
Regioselective functionalization. 6. Migratory preferences in hydroxylamine-O-sulfonic acid and Schmidt rearrangements of 7-substituted norcamphors
Krow, Grant R.,Cheung, Osbert H.,Hu, Zilun,Lee, Yoon B.
, p. 5574 - 5580 (2007/10/03)
Hydroxylamine-O-sulfonic acid reacted with syn-7-X- and anti-7-Y-substituted norcamphor derivatives [X = H, OMe, Cl, Br, OTos; Y = H, COOMe, Cl, Br, Tos, COOMe(5-exo-Br)], to give solely bridgehead migrated 2-azalactams, except for minor amounts of methyl
Magnetic resonance studies of the structure and the red photolysis reactions of 2-chloro-2-nitrosonorbornane
Boucenna, Mohamed-Cherif,Davidson, John S.,McKee, Anthony,Porte, Andrew L.,Apperley, David C.
, p. 1381 - 1388 (2007/10/02)
Detailed NMR studies have shown that at 298 K optically-inactive saturated blue solutions of 2-chloro-2-nitrosonorbornane in CDCl3 contain a mixture of the monomeric and dimeric forms of the compound in a ratio of dimer: monomer=1:40(+/-2): this ratio changes with a change in temperature.The analysis assigns the configuration at the C(2)(NO)(Cl) centre and shows that the monomeric form has the structure (4), in which the NO group is on the same side of the molecule as the bridging C(7)H2 group.White, solid 2-chloro-2-nitrosorbornane is a 1:1:1:1 mixture of four diastereoisomeric forms of trans-diazodioxide (5).The white solid readily sublimes at ambient temperature and monomeric vapour forms a blue-green cast on its surface.Red-irradiation of the compound, in vacuo, produces white crystals and a viscous brown oil.The white crystals contain norbornan-2-one (6), the syn- and anti-forms of the norbornan-2-one oximes, (7) and (8), and a lactam, (9).These compounds are present in the viscous brown oil which also contains three other compounds to which the structures (10), (11) and (12) are assigned.The reaction mixture is EPR silent.The spectrocsopic evidence enables some of the steps in the red photolysis reactions of (4) to be unravelled.
BECKMANN REARRANGEMENTS IN THE BICYCLOHEPTAN-2-ONE SERIES
Hunt, Peter A.,Moody, Christopher J.
, p. 7233 - 7234 (2007/10/02)
In contrast to norcamphor oxime (2), the E-oxime (6), derived from the acetonide of 5,6-dihydroxybicycloheptan-2-one, undergoes regiospecific Beckmann rearrangement to give the lactam (7).
