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14
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85033814955
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note
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Molecular mechanics calculations have pointed out [11] that the preferred conformation of 1b is a fold form favourably arranged for cyclization.
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15
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85033810964
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work in progress, preliminary data have been presented Italy, September
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M. Pani, M. M. Carnasciali, A. Mugnoli, R. Noto, and M. Gruttadauria, work in progress, preliminary data have been presented at XXIV Congresso Nazionale of the A.I.C. Pavia, Italy, September 1994.
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Pani, M.1
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16
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17
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85033809129
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note
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15N nmr data collected for compounds 1a-j [14] show that electron-donating and electron-repelling substituents cause an upfield shift for the N(1) nitrogen atom in contrast to the electron-withdrawing substituents.
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19
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0004053307
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N. B. Chapman and J. Shorter, eds, Plenum Press, New York
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O. Exner, in Correlation Analysis in Chemistry, Recent Advances, N. B. Chapman and J. Shorter, eds, Plenum Press, New York, 1978.
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20
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0003956918
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McGraw-Hill, New York, Chapter 11
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L. P. Hammett, Physical Organic Chemistry, 2nd Ed, McGraw-Hill, New York, 1970, Chapter 11.
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0003689936
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Plenum, New York, SNTL, Prague
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O. Exner, in Correlation Analysis of Chemical Data, Plenum, New York, SNTL, Prague, 1988.
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Correlation Analysis of Chemical Data
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Exner, O.1
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22
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85033817329
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note
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The nmr measurements for N-phenylsubstituted acetamides [19] show that substituents affect more strongly the electron density on the oxygen atom than those on the nitrogen atom.
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