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3
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0000384037
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M. S. Pearson, B. J. Jensky, F. H. Greer, J. P. Hagston, N. M. Wells, J. Org. Chem. 1978, 43, 4617.
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Pearson, M.S.1
Jensky, B.J.2
Greer, F.H.3
Hagston, J.P.4
Wells, N.M.5
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5
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-
29344448514
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-
-3, R = ωR = 0.030. CCDC 277444-277447 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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-
-
-
6
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0242560405
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A. Altomare, M. C. Burla, M. Camalli, G. Cascarano, C. Giacovazzo, A. Guagliardi, A. G. G. Moliterni, G. Polidori, R. Spagna, J. Appl. Crystallogr. 1999, 32, 115.
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Altomare, A.1
Burla, M.C.2
Camalli, M.3
Cascarano, G.4
Giacovazzo, C.5
Guagliardi, A.6
Moliterni, A.G.G.7
Polidori, G.8
Spagna, R.9
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8
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29344465427
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-
note
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[1b]
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-
-
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10
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3242679596
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-
Compound (1R,4R)-3 was previously obtained by HPLC separation of a 1:1 mixture of the cis and trans diols obtained in 55 % yield from a four-step sequence from 1(R)-tetralol: D. R. Boyd, N. D. Sharma, N. A. Kerley, G. McConville, C. C. R. Allen, A. J. Blacker, ARKIVOC 2003, 7, 32.
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(2003)
ARKIVOC
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Boyd, D.R.1
Sharma, N.D.2
Kerley, N.A.3
McConville, G.4
Allen, C.C.R.5
Blacker, A.J.6
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11
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3242747469
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E. P. Kündig, T. Lomberget, R. Bragg, C. Poulard, G. Bernardinelli, Chem. Commun. 2004, 1548.
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(2004)
Chem. Commun.
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-
Kündig, E.P.1
Lomberget, T.2
Bragg, R.3
Poulard, C.4
Bernardinelli, G.5
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12
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20744440315
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For a more recent, closely related synthesis of 6, see: D. Möhring, M. Nieger, B. Lewall, K. H. Dötz, Eur. J. Org. Chem. 2005, 2620.
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(2005)
Eur. J. Org. Chem.
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Möhring, D.1
Nieger, M.2
Lewall, B.3
Dötz, K.H.4
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13
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0346273262
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E. P. Kündig, V. Desobry, D. P. Simmons, J. Am. Chem. Soc. 1983, 105, 6962.
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(1983)
J. Am. Chem. Soc.
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Kündig, E.P.1
Desobry, V.2
Simmons, D.P.3
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14
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29344471508
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note
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1H NMR spectroscopic analysis of the crude product mixture showed free naphthoquinone, dihydroxy complex 4, and diketo complex 5 in a ratio of 23:47:30.
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15
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1642426669
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P. G. Gassman, O. M. Rasmy, T. O. Murdock, K. Saito, J. Org. Chem. 1981, 46, 5457.
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(1981)
J. Org. Chem.
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Gassman, P.G.1
Rasmy, O.M.2
Murdock, T.O.3
Saito, K.4
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16
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0032473893
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-
and references therein
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3} unit and the reduction with N-cyclohexyl-2- benzothiazole sulfenamide (CBS) allows kinetic resolution of the racemic complex; see: H.-G. Schmalz, H. Jope, Tetrahedron 1998, 54, 3457, and references therein.
-
(1998)
Tetrahedron
, vol.54
, pp. 3457
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Schmalz, H.-G.1
Jope, H.2
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17
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0032554989
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T. Oriyama, K. Imai, T. Sano, T. Hosoya, Tetrahedron Lett. 1998, 39, 3529.
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(1998)
Tetrahedron Lett.
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Oriyama, T.1
Imai, K.2
Sano, T.3
Hosoya, T.4
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18
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29344475273
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X-ray structure to be published
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X-ray structure to be published.
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