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Nakajima, M.1
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Vlodavsky, I.1
Korner, G.2
Ishai-Michaeli, R.3
Bashkin, P.4
Bar-Shavit, R.5
Fuks, Z.6
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3
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0029019459
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Shiozawa, H.; Takahashi, M.; Takatsu, T.; Kinoshita, T.; Tanzawa, K.; Hosoya, T.; Furuya, K.; Furihata, K.; Seto, H. J. Antibiot. 1995, 48, 357-369.
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Shiozawa, H.1
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Kinoshita, T.4
Tanzawa, K.5
Hosoya, T.6
Furuya, K.7
Furihata, K.8
Seto, H.9
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4
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0000316683
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Takai, K.1
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Nozaki, H.5
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5
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0000959935
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(b) Takai, K.; Tagashira, M.; Kuroda, T.; Oshima, K.; Utimoto, K.; Nozaki, H. J. Am. Chem. Soc. 1986, 108, 6048-6050.
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Takai, K.1
Tagashira, M.2
Kuroda, T.3
Oshima, K.4
Utimoto, K.5
Nozaki, H.6
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6
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33845375686
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(c) Jin, H.; Uenishi, J.; Christ, W. J.; Kishi, Y. J. Am. Chem. Soc. 1986, 108, 5644-5646.
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Jin, H.1
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7
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0000458709
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Trost, B. M., Ed.; Pergamon: Oxford, UK, Chapter 1.6.4
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For a review see: Saccomano, N. A. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon: Oxford, UK, 1991; Vol. 1, Chapter 1.6.4, pp 193-201.
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Comprehensive Organic Synthesis
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Saccomano, N.A.1
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8
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0141709350
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note
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After aldol reaction with acetone, dehydration gave β,γ -unsaturated ester almost exclusively.
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9
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0141709349
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note
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The triflation reaction proceeded with perfect regioselectivity.
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10
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0028343005
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For the esterification step see: Santini, C.; Ball, R. G.; Berger, G. D. J. Org. Chem. 1994, 59, 2261-2266.
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(1994)
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Santini, C.1
Ball, R.G.2
Berger, G.D.3
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12
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0030754285
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In this particular case, use of 4-tert-butylpyridine as an additive turned out to decrease the yield of the coupling product (<60%). For the procedure with 4-tert-butylpyridine see: Sheng, D. P. X. C.; Chen, S. S.; Kishi, Y. Tetrahedron Lett. 1997, 38, 6355-6358.
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(1997)
Tetrahedron Lett.
, vol.38
, pp. 6355-6358
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Sheng, D.P.X.C.1
Chen, S.S.2
Kishi, Y.3
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13
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0141820644
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note
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When DMSO was used as a solvent, the coupling reaction became very sluggish.
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