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Hagiwara, H.1
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0000758747
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Sarabèr, F.C.E.1
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19
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0001732861
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37049083230
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31
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31444447404
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note
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The concentrations used here are lower than those used in the references cited.
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40
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21644461560
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A. Sobolev, M. Vos, H. Zuilhof, F.C.E. Saraber, B.J.M. Jansen, and A. de Groot Arkivoc 2005 29 part (xiv)
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Sobolev, A.1
Vos, M.2
Zuilhof, H.3
Saraber, F.C.E.4
Jansen, B.J.M.5
De Groot, A.6
-
41
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0012207492
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Ananchenko, S.N.1
Limanov, V.Y.2
Leonov, V.N.3
Rzheznikov, V.N.4
Torgov, I.V.5
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46
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31444435249
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G. Quinkert, M. Del Grosso, A. Döring, W. Döring, R.I. Schenkel, M. Bauch, G.T. Dambacher, J.W. Bats, G. Zimmermann, and G. Dürner Helv. Chim. Acta 1995 78
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Quinkert, G.1
Del Grosso, M.2
Döring, A.3
Döring, W.4
Schenkel, R.I.5
Bauch, M.6
Dambacher, G.T.7
Bats, J.W.8
Zimmermann, G.9
Dürner, G.10
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52
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0021285595
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K.M.R. Pillai, W.V. Murray, I. Shooshani, D.L. Williams, D. Gordon, S.Y. Wang, and F. Johnson J. Med. Chem. 27 1984 1131
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Pillai, K.M.R.1
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Williams, D.L.4
Gordon, D.5
Wang, S.Y.6
Johnson, F.7
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53
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31444434533
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The all-trans configuration of compound 72 was confirmed by X-ray analysis. see: H. Kooijman, F.C.E. Saraber, A. de Groot, and A.L. Spek Acta Crystallogr., Sect. E 61 2005 3908
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Acta Crystallogr., Sect. e
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Kooijman, H.1
Saraber, F.C.E.2
De Groot, A.3
Spek, A.L.4
-
55
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31444443679
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note
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1H NMR shifts of allylic proton due to influence of adjacent phenyl group.
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