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18
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33748600689
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Ref. 1
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For recent work on the synthesis of related spongiane systems, see: (a) Ref. 1; (b) Pattenden, G.; Roberts, L.; Blake, A. J. J. Chem. Soc., Perkin Trans. 1 1998, 863-868; (c) Goeller, F.; Heinemann, C.; Demuth, M. Synthesis 2001, 1114-1116 and references cited therein.
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-
-
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19
-
-
33748600689
-
-
For recent work on the synthesis of related spongiane systems, see: (a) Ref. 1; (b) Pattenden, G.; Roberts, L.; Blake, A. J. J. Chem. Soc., Perkin Trans. 1 1998, 863-868; (c) Goeller, F.; Heinemann, C.; Demuth, M. Synthesis 2001, 1114-1116 and references cited therein.
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(1998)
J. Chem. Soc., Perkin Trans. 1
, pp. 863-868
-
-
Pattenden, G.1
Roberts, L.2
Blake, A.J.3
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20
-
-
0034957110
-
-
and references cited therein
-
For recent work on the synthesis of related spongiane systems, see: (a) Ref. 1; (b) Pattenden, G.; Roberts, L.; Blake, A. J. J. Chem. Soc., Perkin Trans. 1 1998, 863-868; (c) Goeller, F.; Heinemann, C.; Demuth, M. Synthesis 2001, 1114-1116 and references cited therein.
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(2001)
Synthesis
, pp. 1114-1116
-
-
Goeller, F.1
Heinemann, C.2
Demuth, M.3
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22
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0010691569
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-
The stereochemistry of the Diels-Alder adduct formed was assigned on the basis of intramolecular NOE studies. In particular, no NOE was observed upon irradiation of either the Me-8 (δ 1.25 ppm) or the Me-10 (δ 0.98 ppm) on each other, which strongly suggested the anti disposition of both methyl groups.
-
The stereochemistry of the Diels-Alder adduct formed was assigned on the basis of intramolecular NOE studies. In particular, no NOE was observed upon irradiation of either the Me-8 (δ 1.25 ppm) or the Me-10 (δ 0.98 ppm) on each other, which strongly suggested the anti disposition of both methyl groups.
-
-
-
-
24
-
-
0010734680
-
-
-3.
-
-3.
-
-
-
-
25
-
-
0010693224
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-
note
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4′).
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