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7
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0025045174
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Murata, M.1
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Yasumoto, T.7
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12
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30744459350
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Reviews on the total synthesis of ladder-shaped polyethers, see:
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Reviews on the total synthesis of ladder-shaped polyethers, see:. Nakata T. Chem. Rev. 105 (2005) 4314
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Nakata, T.1
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0000563379
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21
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22844434675
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Mori M., Oishi T., Matsuoka S., Ujihara S., Matsumori N., Murata M., Satake M., Oshima Y., Matsushita N., and Aimoto S. Bioorg. Med. Chem. 13 (2005) 5099
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Mori, M.1
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Murata, M.6
Satake, M.7
Oshima, Y.8
Matsushita, N.9
Aimoto, S.10
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22
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33750738565
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Torikai K., Yari H., Mori M., Ujihara S., Matsumori N., Murata M., and Oishi T. Bioorg. Med. Chem. Lett. 16 (2006) 6355
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-
23
-
-
0000733792
-
-
There are few naturally occurring cis-fused cyclic ethers, e.g. dactomelynes, elatenyne, and the LM and NO ring system of maitotoxin.
-
There are few naturally occurring cis-fused cyclic ethers, e.g. dactomelynes, elatenyne, and the LM and NO ring system of maitotoxin. Gopichand Y., Schmitz F.J., Shelley J., Rahman A., and Van der Helm D. J. Org. Chem. 46 (1981) 5192
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Gopichand, Y.1
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25
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-
0000547857
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Murata M., Naoki H., Matsunaga S., Satake M., and Yasumoto T. J. Am. Chem. Soc. 116 (1994) 7098
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Murata, M.1
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-
26
-
-
0001339910
-
-
Convergent synthesis of 7/7 and 6/7 cis-fused ring system by means of hydroxy ketone cyclization, see:
-
Convergent synthesis of 7/7 and 6/7 cis-fused ring system by means of hydroxy ketone cyclization, see:. Nicolaou K.C., Reddy K.R., Skokotas G., Sato F., Xiao X.-Y., and Hwang C.-K. J. Am. Chem. Soc. 115 (1993) 3558
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Nicolaou, K.C.1
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Skokotas, G.3
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Xiao, X.-Y.5
Hwang, C.-K.6
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27
-
-
0000485082
-
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Alvarez E., Pérez R., Rico M., Rodríguez R.M., and Martin J.D. J. Org. Chem. 61 (1996) 3003
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Alvarez, E.1
Pérez, R.2
Rico, M.3
Rodríguez, R.M.4
Martin, J.D.5
-
28
-
-
33947625718
-
-
note
-
+).
-
-
-
-
29
-
-
7744246249
-
-
Matsuo G., Kawamura K., Hori N., Matsukura H., and Nakata T. J. Am. Chem. Soc. 126 (2004) 14374
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-
Matsuo, G.1
Kawamura, K.2
Hori, N.3
Matsukura, H.4
Nakata, T.5
-
30
-
-
25844469499
-
-
Clark J.S., Kimber M.C., Robertson J., McErlean C.S.P., and Wilson C. Angew. Chem. Int. Ed. 44 (2005) 6157
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-
Clark, J.S.1
Kimber, M.C.2
Robertson, J.3
McErlean, C.S.P.4
Wilson, C.5
-
37
-
-
85088765820
-
-
note
-
2t-Bu, THF, HMPA; iv) aq. KOH, McOH, THF, 76% (two steps).
-
-
-
-
40
-
-
0037026010
-
-
Uehara H., Oishi T., Inoue M., Shoji M., Nagumo Y., Kosaka M., Le Brazidec J.-Y., and Hirama M. Tetraheadron 58 (2002) 6493
-
(2002)
Tetraheadron
, vol.58
, pp. 6493
-
-
Uehara, H.1
Oishi, T.2
Inoue, M.3
Shoji, M.4
Nagumo, Y.5
Kosaka, M.6
Le Brazidec, J.-Y.7
Hirama, M.8
-
41
-
-
0035925235
-
-
Oishi T., Uehara H., Nagumo Y., Shoji M., Le Brazidec J.-Y., and Hirama M. Chem. Commun. (2001) 381
-
(2001)
Chem. Commun.
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-
-
Oishi, T.1
Uehara, H.2
Nagumo, Y.3
Shoji, M.4
Le Brazidec, J.-Y.5
Hirama, M.6
-
43
-
-
0032481078
-
-
The effect of temperature on the diastereoselectivity is significant and hydroboration at 0°C gave 17 as a major product. Hydroboration using thexylborane did not improve the selectivity.
-
The effect of temperature on the diastereoselectivity is significant and hydroboration at 0°C gave 17 as a major product. Hydroboration using thexylborane did not improve the selectivity. Sasaki M., Fuwa H., Inoue M., and Tachibana K. Tetrahedron Lett. 39 (1998) 9027
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9027
-
-
Sasaki, M.1
Fuwa, H.2
Inoue, M.3
Tachibana, K.4
-
45
-
-
33845182977
-
-
Nicolaou K.C., Prasad C.V.C., Hwang C.-K., Duggan M.E., and Veale C.A. J. Am. Chem. Soc. 111 (1989) 5321
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(1989)
J. Am. Chem. Soc.
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-
-
Nicolaou, K.C.1
Prasad, C.V.C.2
Hwang, C.-K.3
Duggan, M.E.4
Veale, C.A.5
-
47
-
-
85088766307
-
-
note
-
3 or pyridine, did not provide 21.
-
-
-
-
49
-
-
33947691769
-
-
note
-
+).
-
-
-
-
50
-
-
85088766274
-
-
note
-
3) δ 22: 1.26 and 1.10; 23: 1.22 and 1.10; for reference l: 1.23; 2: 1.12;3: 1.13 and 1.11.
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