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1
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0032775515
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Braekman J.-C., Charlier A., Daloze D., Heilporn S., Pasteels J., Plasman V., and Wang S. Eur. J. Org. Chem. (1999) 1749-1755
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(1999)
Eur. J. Org. Chem.
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Braekman, J.-C.1
Charlier, A.2
Daloze, D.3
Heilporn, S.4
Pasteels, J.5
Plasman, V.6
Wang, S.7
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6
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2342663631
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Rougnon-Glasson S., Tratrat Ch., Canet J.-L., Chalard P., and Troin Y. Tetrahedron: Asymmetry 15 (2004) 1561-1567
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(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 1561-1567
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Rougnon-Glasson, S.1
Tratrat, Ch.2
Canet, J.-L.3
Chalard, P.4
Troin, Y.5
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8
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0001087501
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Tamaru Y., Kobayashi T., Kawamura S.-I., Ochiai H., and Yoshida Z.-I. Tetrahedron Lett. 26 (1985) 4479-4482
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(1985)
Tetrahedron Lett.
, vol.26
, pp. 4479-4482
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Tamaru, Y.1
Kobayashi, T.2
Kawamura, S.-I.3
Ochiai, H.4
Yoshida, Z.-I.5
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13
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0034733620
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Szolcsányi P., Gracza T., Koman M., Prónayová N., and Liptaj T. Tetrahedron: Asymmetry 11 (2000) 2579-2597
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(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 2579-2597
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Szolcsányi, P.1
Gracza, T.2
Koman, M.3
Prónayová, N.4
Liptaj, T.5
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14
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0032489027
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Compound 4 is known in optically pure form as the (S)-enantiomer:
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Compound 4 is known in optically pure form as the (S)-enantiomer:. Fürstner A., and Müller T. J. Org. Chem. 63 (1998) 424-425
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(1998)
J. Org. Chem.
, vol.63
, pp. 424-425
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Fürstner, A.1
Müller, T.2
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17
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38349104236
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Formation of undesired ketone 5 could be explained by a Meerwein-Ponndorf-Verley-type mechanism, see:
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Formation of undesired ketone 5 could be explained by a Meerwein-Ponndorf-Verley-type mechanism, see:. Kovalev B.G., Chusid A.Ch., Konyuchov V.P., Nedopekina C.F., and Neymark J.L. Zh. Org. Khim. 11 (1975) 1183-1187
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(1975)
Zh. Org. Khim.
, vol.11
, pp. 1183-1187
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Kovalev, B.G.1
Chusid, A.Ch.2
Konyuchov, V.P.3
Nedopekina, C.F.4
Neymark, J.L.5
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18
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38349162831
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note
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-1): 666, 815, 905, 1097, 1176, 1188, 1362, 2862, 2932, 2954.
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19
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38349130461
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note
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-1): 910, 1062, 1459, 1641, 2858, 2929, 3077, 3313.
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20
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0030857814
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An identical sequence on analogous compounds is reported, see:
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An identical sequence on analogous compounds is reported, see:. Fürstner A., and Langemann K. Synthesis (1997) 792-803
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(1997)
Synthesis
, pp. 792-803
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Fürstner, A.1
Langemann, K.2
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21
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38349103038
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note
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3N = 86/14/1) yielded three fractions: oxazolidinone 7 as a yellowish oil (5 mg, 4%), calvine rac-1 as a yellowish oil (45 mg, 38%) and epicalvine rac-2 as a yellowish oil (20 mg, 17%).
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22
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38349090171
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2 (239.21): C, 70.25; H, 10.53; N, 5.85%. Found: C, 70.20; H, 10.58; N, 5.88%.
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23
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0004994046
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Preparation of N-substituted oxazolidinones via Pd(II)-catalysed carbonylation of 1,2-aminoalcohols is known:
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Preparation of N-substituted oxazolidinones via Pd(II)-catalysed carbonylation of 1,2-aminoalcohols is known:. Tam W. J. Org. Chem. 51 (1986) 2977-2981
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(1986)
J. Org. Chem.
, vol.51
, pp. 2977-2981
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Tam, W.1
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