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1
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0030742636
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Ishiyama, H.; Ishibashi, M.; Ogawa, A.; Yoshida, S.; Kobayashi, J. J. Org. Chem. 1997, 62, 3831-3836
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Ishiyama, H.1
Ishibashi, M.2
Ogawa, A.3
Yoshida, S.4
Kobayashi, J.5
-
2
-
-
77953581573
-
-
Total syntheses
-
Total syntheses
-
-
-
-
5
-
-
0141905871
-
-
Hollowood, C. J.; Yamanoi, S.; Ley, S. V. Org. Biomol. Chem. 2003, 1, 1664-1675
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(2003)
Org. Biomol. Chem.
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-
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Hollowood, C.J.1
Yamanoi, S.2
Ley, S.V.3
-
6
-
-
77953571245
-
-
Formal syntheses
-
Formal syntheses
-
-
-
-
7
-
-
0035623876
-
-
Zheng, G. R.; Lu, W.; Cai, J. C. Chin. Chem. Lett. 2001, 12, 961-964
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(2001)
Chin. Chem. Lett.
, vol.12
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Zheng, G.R.1
Lu, W.2
Cai, J.C.3
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9
-
-
19744371518
-
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Moreau, X.; Bazan-Tejeda, B.; Campagne, J. M. J. Am. Chem. Soc. 2005, 127, 7288-7289
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Moreau, X.1
Bazan-Tejeda, B.2
Campagne, J.M.3
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11
-
-
0034373768
-
-
See also
-
See also: Zheng, G. R.; Lu, W.; Cai, J. C. Chin. Chem. Lett. 2000, 11, 663-664
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(2000)
Chin. Chem. Lett.
, vol.11
, pp. 663-664
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-
Zheng, G.R.1
Lu, W.2
Cai, J.C.3
-
13
-
-
0001249486
-
-
Chen, K.-M.; Hardtmann, G. E.; Prasad, K.; Repic, O.; Shapiro, M. J. Tetrahedron Lett. 1987, 28, 155-158
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(1987)
Tetrahedron Lett.
, vol.28
, pp. 155-158
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-
Chen, K.-M.1
Hardtmann, G.E.2
Prasad, K.3
Repic, O.4
Shapiro, M.J.5
-
14
-
-
0032482316
-
-
Phosphonate 10 was prepared according to the procedure described in
-
Phosphonate 10 was prepared according to the procedure described in: Cushman, M.; Casimiro-Garcia, A.; Hejchman, E.; Ruell, J. A.; Huang, M.; Schaeffer, C. A.; Williamson, K.; Rice, W. G.; Buckheit, R. W., Jr. J. Med. Chem. 1998, 41, 2076-2089
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(1998)
J. Med. Chem.
, vol.41
, pp. 2076-2089
-
-
Cushman, M.1
Casimiro-Garcia, A.2
Hejchman, E.3
Ruell, J.A.4
Huang, M.5
Schaeffer, C.A.6
Williamson, K.7
Rice, W.G.8
Buckheit Jr., R.W.9
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15
-
-
4444276636
-
-
Kolb, H. C.; Van Nieuwenhze, M. S.; Sharpless, K. B. Chem. Rev. 1994, 94, 2483-2547
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(1994)
Chem. Rev.
, vol.94
, pp. 2483-2547
-
-
Kolb, H.C.1
Van Nieuwenhze, M.S.2
Sharpless, K.B.3
-
16
-
-
9644292316
-
-
For example: borohydride reduction of the cyclic sulfite/sulfate
-
For example: borohydride reduction of the cyclic sulfite/sulfate: Gao, Y.; Sharpless, K. B. J. Am. Chem. Soc. 1988, 110, 7538-7539
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 7538-7539
-
-
Gao, Y.1
Sharpless, K.B.2
-
17
-
-
0035898783
-
-
Upadhya, T. T.; Nikalje, M. D.; Sudalai, A. Tetrahedron Lett. 2001, 42, 4891-4893
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4891-4893
-
-
Upadhya, T.T.1
Nikalje, M.D.2
Sudalai, A.3
-
18
-
-
0025291224
-
-
Iodide-mediated reduction of the α-triflate
-
Iodide-mediated reduction of the α-triflate: Elliott, R. P.; Fleet, G. W. J.; Gyoung, Y. S.; Ramsden, N. G.; Smith, C. Tetrahedron Lett. 1990, 31, 3785-3788
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(1990)
Tetrahedron Lett.
, vol.31
, pp. 3785-3788
-
-
Elliott, R.P.1
Fleet, G.W.J.2
Gyoung, Y.S.3
Ramsdenn., G.4
Smith, C.5
-
19
-
-
0000676113
-
-
Reduction of the α-mesylate: [Na(Hg)]
-
Reduction of the α-mesylate: [Na(Hg)]: Stork, G.; Rychnovsky, S. D. J. Am. Chem. Soc. 1987, 109, 1564-1565
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 1564-1565
-
-
Stork, G.1
Rychnovsky, S.D.2
-
21
-
-
0030841601
-
-
Selenide reduction of the α,β-epoxide
-
Selenide reduction of the α,β-epoxide: Miyashita, M.; Suzuki, T.; Hoshino, M.; Yoshikoshi, A. Tetrahedron 1997, 53, 12469-12486
-
(1997)
Tetrahedron
, vol.53
, pp. 12469-12486
-
-
Miyashita, M.1
Suzuki, T.2
Hoshino, M.3
Yoshikoshi, A.4
-
23
-
-
77953547553
-
-
2O; (c) TsCl, pyridine; (d) LiBr, acetone (38% overall); step (d) has to be performed with care to avoid alkene isomerization and loss of the volatile product during isolation
-
2O; (c) TsCl, pyridine; (d) LiBr, acetone (38% overall); step (d) has to be performed with care to avoid alkene isomerization and loss of the volatile product during isolation.
-
-
-
-
24
-
-
0032569909
-
-
Smith, A. B., III; Cho, Y. S.; Friestad, G. K. Tetrahedron Lett. 1998, 39, 8765-8768
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8765-8768
-
-
Smith Iii, A.B.1
Cho, Y.S.2
Friestad, G.K.3
-
25
-
-
0034697701
-
-
Nishimura, T.; Kakiuchi, N.; Onoue, T.; Ohe, K.; Uemura, S. J. Chem. Soc., Perkin Trans. 1 2000, 1915-1918
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(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 1915-1918
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-
Nishimura, T.1
Kakiuchi, N.2
Onoue, T.3
Ohe, K.4
Uemura, S.5
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26
-
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0001890076
-
-
Wiley: New York,; Collect.
-
Tsuji, J.; Nagashima, H.; Nemoto, H. Organic Syntheses; Wiley: New York, 1990; Collect. Vol. VII, pp 137 - 139.
-
(1990)
Organic Syntheses
, vol.7
, pp. 137-139
-
-
Tsuji, J.1
Nagashima, H.2
Nemoto, H.3
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27
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66749093013
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-
Tietze, L. F.; Kinzel, T.; Wolfram, T. Chem.-Eur. J. 2009, 15, 6199-6210
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(2009)
Chem.-Eur. J.
, vol.15
, pp. 6199-6210
-
-
Tietze, L.F.1
Kinzel, T.2
Wolfram, T.3
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28
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77953547854
-
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We are very grateful to Professor Tietze and his group for their invaluable advice in relation to this procedure
-
We are very grateful to Professor Tietze and his group for their invaluable advice in relation to this procedure.
-
-
-
-
29
-
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77953595191
-
-
13C NMR spectrum for 17 were doubled, including that at 34.6 ppm, which was sensitive to stereochemical change (34.4 ppm in the adduct generated using the (S)-configured auxiliary)
-
13C NMR spectrum for 17 were doubled, including that at 34.6 ppm, which was sensitive to stereochemical change (34.4 ppm in the adduct generated using the (S)-configured auxiliary).
-
-
-
-
30
-
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77953551498
-
-
We will report further details in a full description of this work
-
We will report further details in a full description of this work.
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-
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31
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0001409192
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Scheidt, K. A.; Chen, H.; Follows, B. C.; Chemler, S. R.; Coffey, D. S.; Roush, W. R. J. Org. Chem. 1998, 63, 6436-6437
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(1998)
J. Org. Chem.
, vol.63
, pp. 6436-6437
-
-
Scheidt, K.A.1
Chen, H.2
Follows, B.C.3
Chemler, S.R.4
Coffey, D.S.5
Roush, W.R.6
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32
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77953579874
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Chemistry Part II Thesis, Oxford
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Reynolds, L. Chemistry Part II Thesis, Oxford, 2008.
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(2008)
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Reynolds, L.1
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