-
3
-
-
85030196266
-
-
note
-
β-Keto phosphine oxide 9 was synthesised in 52% yield using an acylation reaction between lithiated methyldiphenylphosphine oxide and methyl ester 6.
-
-
-
-
4
-
-
0000870492
-
-
He, X-C.; Eliel, E. L. Tetrahedron, 1987, 43, 4979-4987. See also: Matsubara, S.; Takahashi, H.; Utimoto, K. Chem. Lett., 1992, 2173-2176.
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Tetrahedron
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He, X.-C.1
Eliel, E.L.2
-
5
-
-
0011983970
-
-
He, X-C.; Eliel, E. L. Tetrahedron, 1987, 43, 4979-4987. See also: Matsubara, S.; Takahashi, H.; Utimoto, K. Chem. Lett., 1992, 2173-2176.
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Chem. Lett.
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Matsubara, S.1
Takahashi, H.2
Utimoto, K.3
-
6
-
-
0001127065
-
-
Ko, K-Y.; Frazee, W. J.; Eliel, E. L. Tetrahedron, 1984, 40, 1333-1343.
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Tetrahedron
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Ko, K.-Y.1
Frazee, W.J.2
Eliel, E.L.3
-
7
-
-
4544302195
-
-
Manzoni, L.; Pilati, T.; Poli, G.; Scolastico, C. J. Chem. Soc., Chem. Commun., 1992, 1027-1029.
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Manzoni, L.1
Pilati, T.2
Poli, G.3
Scolastico, C.4
-
8
-
-
85032119272
-
-
Poli, G.; Maccagni, E.; Manzoni, L.; Pilati, T.; Scolastico, C. Synlett, 1995, 71-73.
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(1995)
Synlett
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Poli, G.1
Maccagni, E.2
Manzoni, L.3
Pilati, T.4
Scolastico, C.5
-
9
-
-
0028955943
-
-
Agami, C.; Couty, F.; Lequesne, C Tetrahedron, 1995, 51, 4043-4056; Agami, C.; Couty, F.; Lequesne, C. Tetrahedron Lett., 1994, 35, 3309-3312; Colombo, L.; Di Giacomo, M.; Brusotti, G.; Delogu, G. Tetrahedon Lett., 1994, 35, 2063-2066.
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(1995)
Tetrahedron
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, pp. 4043-4056
-
-
Agami, C.1
Couty, F.2
Lequesne, C.3
-
10
-
-
0028240876
-
-
Agami, C.; Couty, F.; Lequesne, C Tetrahedron, 1995, 51, 4043-4056; Agami, C.; Couty, F.; Lequesne, C. Tetrahedron Lett., 1994, 35, 3309-3312; Colombo, L.; Di Giacomo, M.; Brusotti, G.; Delogu, G. Tetrahedon Lett., 1994, 35, 2063-2066.
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(1994)
Tetrahedron Lett.
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, pp. 3309-3312
-
-
Agami, C.1
Couty, F.2
Lequesne, C.3
-
11
-
-
0028354084
-
-
Agami, C.; Couty, F.; Lequesne, C Tetrahedron, 1995, 51, 4043-4056; Agami, C.; Couty, F.; Lequesne, C. Tetrahedron Lett., 1994, 35, 3309-3312; Colombo, L.; Di Giacomo, M.; Brusotti, G.; Delogu, G. Tetrahedon Lett., 1994, 35, 2063-2066.
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(1994)
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, vol.35
, pp. 2063-2066
-
-
Colombo, L.1
Di Giacomo, M.2
Brusotti, G.3
Delogu, G.4
-
12
-
-
0026323731
-
-
Hoppe, I.; Hoffmann, H.; Gärtner, I.; Kretteck, T.; Hoppe, D. Synthesis, 1991, 1157-1162.
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(1991)
Synthesis
, pp. 1157-1162
-
-
Hoppe, I.1
Hoffmann, H.2
Gärtner, I.3
Kretteck, T.4
Hoppe, D.5
-
13
-
-
0000439882
-
-
For the experimental procedure used, see: Bernardi, A.; Cardani, S.; Pilati, T.; Poli, G.; Scolastico, C.; Villa, R. J. Org. Chem., 1988, 53, 1600-1607.
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(1988)
J. Org. Chem.
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, pp. 1600-1607
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-
Bernardi, A.1
Cardani, S.2
Pilati, T.3
Poli, G.4
Scolastico, C.5
Villa, R.6
-
14
-
-
85030186798
-
-
note
-
Scolastico synthesised essentially the same ratio of 1,2 diols syn- and anti-11 in 80% yield using a slightly different dihydroxylation procedure (see reference 6).
-
-
-
-
15
-
-
85030191884
-
-
note
-
2) and the hydroxyl group as drawn.
-
-
-
-
16
-
-
0028954582
-
-
Eames, J.; Mitchell, H. J.; Nelson, A.; O'Brien, P.; Warren, S.; Wyatt, P. Tetrahedron Lett., 1995, 36, 1719-1722.
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(1995)
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-
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Eames, J.1
Mitchell, H.J.2
Nelson, A.3
O'Brien, P.4
Warren, S.5
Wyatt, P.6
-
19
-
-
0026459980
-
-
For a review on the use of cyclic sulfates and sulfites in synthesis, see: Lohray, B. B. Synthesis, 1992, 1035-1052; Kolb, H. C., VanNieuwenhze, M. S.; Sharpless, K. B. Chem. Rev., 1994, 94, 2483-2547.
-
(1992)
Synthesis
, pp. 1035-1052
-
-
Lohray, B.B.1
-
20
-
-
4444276636
-
-
For a review on the use of cyclic sulfates and sulfites in synthesis, see: Lohray, B. B. Synthesis, 1992, 1035-1052; Kolb, H. C., VanNieuwenhze, M. S.; Sharpless, K. B. Chem. Rev., 1994, 94, 2483-2547.
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, pp. 2483-2547
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Kolb, H.C.1
VanNieuwenhze, M.S.2
Sharpless, K.B.3
-
21
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-
0000751744
-
-
Ashby, E. C.; Gurumurthy, R.; Ridlehuber, R. W. J. Org. Chem., 1993, 58, 5832-5837. For another example of our use of lithium diphenylphosphide prepared in this way, see: O'Brien, P.; Warren, S. Tetrahedron Lett., 1995, 36, 8473-8476.
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J. Org. Chem.
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, pp. 5832-5837
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Ashby, E.C.1
Gurumurthy, R.2
Ridlehuber, R.W.3
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22
-
-
0028848616
-
-
Ashby, E. C.; Gurumurthy, R.; Ridlehuber, R. W. J. Org. Chem., 1993, 58, 5832-5837. For another example of our use of lithium diphenylphosphide prepared in this way, see: O'Brien, P.; Warren, S. Tetrahedron Lett., 1995, 36, 8473-8476.
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(1995)
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O'Brien, P.1
Warren, S.2
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25
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33947094130
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Luche, J-L. J. Am. Chem. Soc., 1978, 100, 2226-2227; Gemal, A. L.; Luche, J-L., J. Am. Chem. Soc., 1981, 103, 5454-5459.
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Luche, J.-L.1
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26
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33845556313
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Luche, J-L. J. Am. Chem. Soc., 1978, 100, 2226-2227; Gemal, A. L.; Luche, J-L., J. Am. Chem. Soc., 1981, 103, 5454-5459.
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Gemal, A.L.1
Luche, J.-L.2
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27
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0001886121
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Frieboes, K. C.; Harder, T.; Aulbert, D.; Strahringer, C,; Bolte, M.; Hoppe, D. Synlett, 1993, 921-923.
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Synlett
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Frieboes, K.C.1
Harder, T.2
Aulbert, D.3
Strahringer, C.4
Bolte, M.5
Hoppe, D.6
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28
-
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0028803867
-
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Chelation of cerium between ketone and phosphinoyl oxygens in Luche reductions is well established: Hutton, G.; Jolliff, T.; Mitchell, H.; Warren, S. Tetrahedron Lett., 1995, 36, 7905-7908.
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Hutton, G.1
Jolliff, T.2
Mitchell, H.3
Warren, S.4
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30
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0027939635
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For an alternative electrochemical method of deprotection of oxazolidines, see: Harder, T.; Löhl, T.; Bolte, M.; Wagner, K.; Hoppe, D. Tetrahedron Lett., 1994, 35, 7365-7368.
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(1994)
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Harder, T.1
Löhl, T.2
Bolte, M.3
Wagner, K.4
Hoppe, D.5
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Pirkte, W. H.; Sikkenga, D. L.; Pavlin, D. S.; J. Org. Chem., 1977, 42, 384-387.
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Pavlin, D.S.3
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