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1
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0003799267
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in: P.J. Stang, F. Diederich, (Eds.) VCH, Weinheim
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K.C. Nicolaou, A.L. Smith, in: P.J. Stang, F. Diederich, (Eds.), Modern Acetylene Chemistry, VCH, Weinheim 1995.
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Modern Acetylene Chemistry
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Nicolaou, K.C.1
Smith, A.L.2
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2
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0030005845
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(a)
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(a) J.W. Grissom, G.U. Gunawardena, D. Klingberg, D. Huang, Tetrahedron 52 (1996) 6453.
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Grissom, J.W.1
Gunawardena, G.U.2
Klingberg, D.3
Huang, D.4
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5
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84883839798
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(a)
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(a) N. Ishida, K. Miyazaki, K.M. Kumagai, M.J. Rikimura, Antibiotics 18 (1965) 68.
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Antibiotics
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Ishida, N.1
Miyazaki, K.2
Kumagai, K.M.3
Rikimura, M.J.4
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6
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0021960376
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(b) - the first synthesis of the NCS-Chr aglycone has recently been described
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(b) K. Edo, M. Mizugaki, Y. Koide, H. Seto, K. Furihata, N. Otake, N. Ishida, Tetrahedron Lett. 26 (1985) 331 - the first synthesis of the NCS-Chr aglycone has recently been described:
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Tetrahedron Lett.
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Edo, K.1
Mizugaki, M.2
Koide, Y.3
Seto, H.4
Furihata, K.5
Otake, N.6
Ishida, N.7
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7
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0029956497
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(c)
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(c) A.G. Myers, M. Hammond, Y. Wu, J.-N. Xiang, P.M. Harrington, E.Y. Kuo, J. Am. Chem. Soc. 118 (1996) 10006.
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(1996)
J. Am. Chem. Soc.
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Myers, A.G.1
Hammond, M.2
Wu, Y.3
Xiang, J.-N.4
Harrington, P.M.5
Kuo, E.Y.6
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9
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4243557015
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Jpn. Kokai Tokkyo Koho JP 07291955
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M. Ishii, T. Ando, T. Kajiura, T. Kameyama, Y Nihey, Jpn. Kokai Tokkyo Koho JP 07291955, Chem. Abstr. 124 (1996) 115564h.
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Ishii, M.1
Ando, T.2
Kajiura, T.3
Kameyama, T.4
Nihey, Y.5
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10
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0000509322
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(a) in: I. Fleming, B.M. Trost, (Eds.) Pergamon, Oxford
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(a) K. Sonogashira, in: I. Fleming, B.M. Trost, (Eds.), Comprehensive Organic Chemistry, vol.3, Pergamon, Oxford, 1991 pp 521.
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(1991)
Comprehensive Organic Chemistry
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Sonogashira, K.1
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11
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0001058604
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(b) in: E.W. Abel, F.G.A. Stone, G. Wilkinson, (Eds.) Pergamon, Oxford
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(b) V. Farina, in: E.W. Abel, F.G.A. Stone, G. Wilkinson, (Eds.), Comprehensive Organometallic Chemistry II, vol. 12, Pergamon, Oxford, 1995, pp 222.
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Comprehensive Organometallic Chemistry II
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Farina, V.1
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18
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0023838949
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(c)
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(c) E.J. Corey, M.C. Kang, M.C. Desai, A.K. Ghosh, I.N. Houpis, J. Am. Chem. Soc. 10 (1988) 649.
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Corey, E.J.1
Kang, M.C.2
Desai, M.C.3
Ghosh, A.K.4
Houpis, I.N.5
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24
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0000202518
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Scott W.J., Peña M.R., Swärd K., Stoessel S.J., Stille J.K. J. Org. Chem. 50:1985;2302.
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Scott, W.J.1
Peña, M.R.2
Swärd, K.3
Stoessel, S.J.4
Stille, J.K.5
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27
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0040781324
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This diyne was obtained from propargyl alcohol, see reference 17
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This diyne was obtained from propargyl alcohol, see reference 17.
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28
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0027314212
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This alkyne is easily obtained from the commercially available (Fluka) Z 3-methyl pent-2-en-4-yn-1-ol after mCPBA epoxidation and silylation
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This alkyne is easily obtained from the commercially available (Fluka) Z 3-methyl pent-2-en-4-yn-1-ol after mCPBA epoxidation and silylation. D. Grandjean, P. Pale, J. Chuche, Tetrahedron 49 (1993) 5225.
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(1993)
Tetrahedron
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Grandjean, D.1
Pale, P.2
Chuche, J.3
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29
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0039002901
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This epoxydiyne was obtained from the cis 2,3-epoxy-3-methyl-1-trimethylsilyloxy pent-4-yne. see reference 17
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This epoxydiyne was obtained from the cis 2,3-epoxy-3-methyl-1-trimethylsilyloxy pent-4-yne. see reference 17.
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31
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0003515609
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Vinyl protons at the β-position of α, β-unsaturated ketones in planar s-cis conformation suffer from a high desielding due to the anisotropy of the adjacent carbonyl. See Pergamon, Oxford
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Vinyl protons at the β-position of α, β-unsaturated ketones in planar s-cis conformation suffer from a high desielding due to the anisotropy of the adjacent carbonyl. See L.M. Jackman, Applications of NMR Spectrocopy in Organic Chemistry, Pergamon, Oxford, 1962.
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(1962)
Applications of NMR Spectrocopy in Organic Chemistry
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Jackman, L.M.1
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38
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0001844458
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in: E.W. Abel, F.G.A. Stone, G. Wilkinson, (Eds.) Pergamon, Oxford
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G. Van Koten, S.L. James, J.T.B.H. Jastrzebski,. in: E.W. Abel, F.G.A. Stone, G. Wilkinson, (Eds.), Comprehensive Organometallic Chemistry II, vol. 3, Pergamon, Oxford, 1995, pp 57.
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(1995)
Comprehensive Organometallic Chemistry II
, vol.3
, pp. 57
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Van Koten, G.1
James, S.L.2
Jastrzebski, J.T.B.H.3
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42
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0039002897
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note
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1H-NMR of the crude mixture obtained from alkynes and silver salts in the presence of tertiary amines exhibited changes suggesting the formation of such complexes.
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