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0010586403
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Non systematic numbering is adopted for heterolignans to maintain the accepted numbering for lignans (see ref. 1a and references therein). In this situation, it is assumed that the heteroatom X replaces positions 2 and 3
-
3. Non systematic numbering is adopted for heterolignans to maintain the accepted numbering for lignans (see ref. 1a and references therein). In this situation, it is assumed that the heteroatom X replaces positions 2 and 3.
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33645171714
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4 treatment. No aromatization products were observed for thiophene derivatives in any case
-
4 treatment. No aromatization products were observed for thiophene derivatives in any case.
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See also 8 and references therein
-
b) See also 8 and references therein.
-
-
-
-
32
-
-
0010550187
-
-
1H-NMR spectrum of 5 shows C-7′ and C-8′ as two broad singlets, in agreement with a trans relationship between this pair of protons and a cis relationship between C-8 and C-8′
-
1H-NMR spectrum of 5 shows C-7′ and C-8′ as two broad singlets, in agreement with a trans relationship between this pair of protons and a cis relationship between C-8 and C-8′.
-
-
-
-
33
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0023768503
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13 a) Andrews, R.C.; Teague, S.J.; Meyers, A.I. J. Am. Chem. Soc. 1988, 110, 7854.
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35
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0010620705
-
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ref. 6a
-
c) ref. 6a.
-
-
-
-
36
-
-
0010552861
-
-
note
-
3, 20C MHz) δ 7.27 (d, J = 5.1, 1H); 6.67 (d, J = 5.1, 1H); 6.37 (s, 2H); 4.97 (d, J = 7.7, 1H); 4.60 (d J = 4.0, 1H); 4.50 (dd, J = 6.6, 8.4, 1H); 4.01 (dd, J = 6.8, 8.7, 1H); 3.02-2.86 (m, 2H); 0.94 (s, 9H); 0.27 (s, 3H); 0.11 (s, 3H)
-
-
-
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37
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16044363432
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15. Bertounesque, E.; Imbert, T.; Monneret, C. Tetrahedron 1996, 52, 14235.
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Bertounesque, E.1
Imbert, T.2
Monneret, C.3
-
38
-
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0010585624
-
-
note
-
3 in 2,3-disubstituted thiophene are 125.68° and 123.28° respectively, higher than those for benzene (120° each), further increasing the strain of the 7',8-cis-8,8'-trans cyclolignanolides.
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