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Heaney, F,Rooney, O,Cunningham, D,McArdle, P
2001
January
Journal Of The Chemical Society-Perkin Transactions 2
Simultaneous double 1,3-dipolar cycloaddition reactions involving bisnitrones or bisdipolarophiles. H-1 NMR investigation of the conformational preferences of N-methyl- and N-phenyl-isoxazolidines
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NITRONES MACROCYCLES
373
378
Binitrones 1a and 1b reacted with N-methylmaleimide giving bisisoxazolidines. Diastereospecific reaction of the phenyl substituted dipole 1a gave 3a whilst the N-methyl dipole 1b furnished diastereomeric adducts 3b, 4 and 7 classified as trans,trans, 3b, cis,cis, 4 and cis,trans adducts 7 (major) according to the relative orientation of the 3-H and 4-H protons on each isoxazolidine ring. Similar behaviour was observed in reaction of mono dipoles N-benzylideneaniline N-oxide and N-benzylidenemethylamine N-oxide with phenylenedimaleimide 2. The N-phenyl dipole reacted highly selectively furnishing the trans,trans adduct 8a whilst the N-methyl dipole again gave trans,trans 8b, cis,cis 10 and cis,trans adducts 9 (major). Some of the N-methyl substituted isoxazolidines (3b, 7, 8b, 9b) displayed a number of very broad signals in their rt H-1 NMR spectra which sharpened (and duplicated) on cooling. By analogy to the corresponding H-1 NMR data of the "hemi-adducts" 5 and 6, and with reference to crystal structure data for 5c [Fig. 1], it was shown that for this group of adducts the 3-H and 4-H protons are trans orientated. The isoxazolidine ring in these adducts equilibrates between the o- and i-conformations [Fig. 2] and at -40 degreesC each conformer can be clearly identified in the H-1 NMR spectrum. No line broadening was observed in the H-1 NMR spectra of any of the N-phenyl substituted adducts. The conformational freedom of the adducts is thus dictated by the size of the N-isoxazolidine substituent and the relative orientation of the 3-H and 4-H protons. All new cycloadducts reported, 3-10, are prepared as racemic mixtures and stereochemical information portrayed in the drawings implies relative and not absolute relations.
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