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Johnson, A.W.1
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For representative examples of vinylogous reactions, see; I. Fleming, A. Berbero, D. Walter, Chem. Rev. 1997, 97, 2063-2192
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S. E. Denmark, J. R. Heemstra, Jr., G. L. Beutner, Angew. Chem. 2005, 117, 4760-4777;
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Angew. Chem. Int. Ed. 2005, 44, 4682-4698
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Angew1
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0033690703
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Casiraghi, G.1
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Mannich reaction
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S. K. Bur, S. F. Martin, Tetrahedron 2001, 57, 3221-3242 (Mannich reaction);
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Bur, S.K.1
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0011211458
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Pummerer rearrangement
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A. Padwa, J. T. Kuethe, J. Org. Chem. 1998, 63, 4256-4268 (Pummerer rearrangement);
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Morita-Baylis-Hillman reaction
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Frank, S.A.1
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E. Vedejs, J. P. Bershas, P. L. Fuchs, J. Org. Chem. 1973, 38, 3625-3627;
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c) E. Vedejs, J. P. Bershas, P. L. Fuchs, J. Org. Chem. 1973, 38, 3625-3627;
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33846436660
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f) W. G. Dauben, D. J. Hart, J. Ipaktschi, A. P. Kozikowski, Tetrahedron 1978, 34, 4673-4675;
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i) Md. S. Islam, T. Kawano, M. Hatanaka, I. Ueda, Tetrahedron Lett. 1996, 37, 5735-5738;
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k) M. Hatanaka, Y. Himeda, R. Imashiro, Y. Tanaka, I. Ueda, J. Org. Chem. 1994, 59, 111-119;
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a) S. M. Date, R. Singh, S. K. Ghosh, Org. Biomol. Chem. 2005, 3, 3369-3378;
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49
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0033547964
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The terminology vinylogous HWE reaction was also used for the α condensation of allylic phophonates to aldehydes; see
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The terminology "vinylogous HWE reaction" was also used for the α condensation of allylic phophonates to aldehydes; see: S. R. Chemler, D. S. Coffey, W. R. Roush, Tetrahedron Lett. 1999, 40, 1269-1272.
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Chemler, S.R.1
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53
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33846459850
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The reaction between 8a and benzaldehyde is reported in ref. [9g], but the authors did not observe the formation of 5a or 6a.
-
The reaction between 8a and benzaldehyde is reported in ref. [9g], but the authors did not observe the formation of 5a or 6a.
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-
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56
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84989585272
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For representative examples of approaches based on the Wittig reaction, see: a
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For representative examples of approaches based on the Wittig reaction, see: a) S. E. Denmark, J. Amburgey, J. Am. Chem. Soc. 1993, 115, 10386-10387;
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J. Am. Chem. Soc
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Denmark, S.E.1
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33645025619
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For the synthesis of trisubstituted conjugated dienes, see:, and references therein
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For the synthesis of trisubstituted conjugated dienes, see: G. A. Molander, Y. Yokoyama, J. Org. Chem. 2006, 71, 2493-2498, and references therein.
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Molander, G.A.1
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60
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33846429852
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A mechanistic rationale is provided in the Supporting Information
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A mechanistic rationale is provided in the Supporting Information.
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