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Weyerstahl, P.1
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Hofer, O.1
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7
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33748995892
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note
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First rac-2 should be prepared because in most cases one enantiomer and the racemate smell very similar.
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8
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0001024939
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F. Bohlmann, C. Zdero, J. Jakupovic, H. Robinson, R. M. King, Phytochemistry 1981, 20, 2239-2244.
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Bohlmann, F.1
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King, R.M.5
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9
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0006675568
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F. Bohlmann, C. Zdero, R. M. King, H. Robinson, Phytochemistry 1981, 20, 2425-2427.
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Bohlmann, F.1
Zdero, C.2
King, R.M.3
Robinson, H.4
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11
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0042255640
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F. Bohlmann, P. Singh, J. Jakupovic, Phytochemistry 1982, 21, 157-160.
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Bohlmann, F.1
Singh, P.2
Jakupovic, J.3
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13
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0344149011
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0345136822
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T. M. Khomenko, I. Yu. Bagryanskaya, Yu. V. Gatilov, D. V. Korchagina, V. P. Gatilova, Zh. V. Dubovenko, V. A. Barkash, Zh. Org. Khim. 1985, 21, 677-678
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Khomenko, T.M.1
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15
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33748994231
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[Chem. Abstr. 1985, 103, 123718t].
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Chem. Abstr.
, vol.103
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19
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0342909370
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2: calcd. 214.0761, found 214.0761 (HR MS). - Concomitant electrophilic chlorination affording unwanted α-chloro ketones during the Swern oxidation with oxalyl chloride and DMSO was reported by A. B. Smith, III, T. L. Leenay, Tetrahedron Lett. 1988, 29, 49-52.
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Leenay, T.L.2
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Sakurai, H.1
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23
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-
85087249255
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-
note
-
1,8 = 6 Hz) for 8-H proved the cis position of 1-H and 8-H and the trans position of 7-H and 8-H.
-
-
-
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24
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0003099695
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R. L. Settine, G. L. Parks, G. L. K. Hunter, J. Org. Chem. 1964, 29, 616-618.
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Settine, R.L.1
Parks, G.L.2
Hunter, G.L.K.3
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27
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0000790988
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Commercially available. For preparation of bromo acetal 7 see also Org. Synth. 1984, 62, 140-148.
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Org. Synth.
, vol.62
, pp. 140-148
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-
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28
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0002094569
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P. Brougham, M. S. Cooper, D. A. Cummerson, H. Heaney, N. Thompson, Synthesis 1987, 1015-1017.
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Brougham, P.1
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Heaney, H.4
Thompson, N.5
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29
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0030039072
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D = -31.5) was isolated also from A. chamaemelifolia: J. A. Marco, J. F. Sanz-Cervera, M. D. Morante, V. García-Lliso, J. Vallès-Xirau, J. Jacunovic, Phytochemistry 1996, 41, 837-844.
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Marco, J.A.1
Sanz-Cervera, J.F.2
Morante, M.D.3
García-Lliso, V.4
Vallès-Xirau, J.5
Jacunovic, J.6
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