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1
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0000598624
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doi:10.1071/CH99082
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L. Aurelio, R. T. C. Brownlee, A. B. Hughes, B. E. Sleebs, Aust. J. Chem. 2000, 53, 425. doi:10.1071/CH99082
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Aurelio, L.1
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2
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0037126285
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L. Aurelio, R. T. C. Brownlee, A. B. Hughes, Org. Lett. 2002, 4, 3767. doi:10.1021/OL026799W
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Box, J.S.2
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Hughes, A.B.4
Sleebs, M.M.5
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4
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11144336770
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L. Aurelio, R. T. C. Brownlee, A. B. Hughes, Chem. Rev. 2004, 104, 5823. doi:10.1021/CR030024Z
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18744372444
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Hughes, A.B.1
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Aurelio, L.3
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9
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39049107344
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A. B. Hughes, B. E. Sleebs, Aust. J. J. Chem. 2008, 61, 131.
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A. B. Hughes, B. E. Sleebs, Aust. J. J. Chem. 2008, 61, 131.
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10
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0029083522
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doi:10.1021/JO00122A010
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K. K. Lee, J. B. Gloer, J. A. Scott, D. Malloch, J. Org. Chem. 1995, 60, 5384. doi:10.1021/JO00122A010
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, pp. 5384
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Lee, K.K.1
Gloer, J.B.2
Scott, J.A.3
Malloch, D.4
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11
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33745802361
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L. Aurelio, R. T. C. Brownlee, J. Dang, J. B. Gloer, A. B. Hughes G. M. Polya, Aust. J. Chem. 2006, 59, 407. doi:10.1071/CH06148
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L. Aurelio, R. T. C. Brownlee, J. Dang, J. B. Gloer, A. B. Hughes G. M. Polya, Aust. J. Chem. 2006, 59, 407. doi:10.1071/CH06148
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-
-
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12
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33749568589
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doi:10.1039/B608434F
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J. Dang, L. Aurelio, A. B. Hughes, R. T. C. Brownlee, Org. Biomol. Chem. 2006, 4, 3802. doi:10.1039/B608434F
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Dang, J.1
Aurelio, L.2
Hughes, A.B.3
Brownlee, R.T.C.4
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13
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-
49749133141
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-
Compounds 9, 13, and 55 were commercial products.
-
Compounds 9, 13, and 55 were commercial products.
-
-
-
-
14
-
-
49749140056
-
-
3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 10.
-
3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 10.
-
-
-
-
15
-
-
0026783997
-
-
Compound 12 was prepared from racemic pipecolinic acid by resolution via tartrate salts (D. S. Perlow, J. M. Erb, N. P. Gould, R. D. Tung, R. M. Freidinger, P. D. Williams, D. F. Veber, J. Org. Chem. 1992, 57, 4394).
-
Compound 12 was prepared from racemic pipecolinic acid by resolution via tartrate salts (D. S. Perlow, J. M. Erb, N. P. Gould, R. D. Tung, R. M. Freidinger, P. D. Williams, D. F. Veber, J. Org. Chem. 1992, 57, 4394).
-
-
-
-
16
-
-
84988088747
-
-
The resolved salt was then carbamoylated E. Ponnusamy, U. Fotadar, A. Spisni, D. Fiat, Synthesis 1986, 48;
-
The resolved salt was then carbamoylated (E. Ponnusamy, U. Fotadar, A. Spisni, D. Fiat, Synthesis 1986, 48;
-
-
-
-
17
-
-
49749115184
-
-
3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 12.
-
3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 12.
-
-
-
-
18
-
-
0001023731
-
-
Compound 15 was identical to material described by
-
Compound 15 was identical to material described by J. R. McDermott, N. L. Benoiton, Can. J. Chem. 1973, 51, 1915.
-
(1973)
Can. J. Chem
, vol.51
, pp. 1915
-
-
McDermott, J.R.1
Benoiton, N.L.2
-
19
-
-
0001001070
-
-
Compound 17 was identical to material described by
-
Compound 17 was identical to material described by S. T. Cheung, N. L. Benoiton, Can. J. Chem. 1977, 55, 906.
-
(1977)
Can. J. Chem
, vol.55
, pp. 906
-
-
Cheung, S.T.1
Benoiton, N.L.2
-
20
-
-
37049078981
-
-
doi:10.1039/P19930000011
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F. Degerbeck, B. Fransson, L. Grehn, U. Ragnarsson, J. Chem. Soc., Perkin Trans. 1 1993, 11. doi:10.1039/P19930000011
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Degerbeck, F.1
Fransson, B.2
Grehn, L.3
Ragnarsson, U.4
-
21
-
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0242391681
-
-
doi:10.1021/JO01266A112
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T. Mizoguchi, G. Levin, D. W. Woolley, J. M. Stewart, J. Org. Chem. 1968, 33, 903. doi:10.1021/JO01266A112
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, pp. 903
-
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Mizoguchi, T.1
Levin, G.2
Woolley, D.W.3
Stewart, J.M.4
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22
-
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37049109112
-
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doi:10.1039/P19850002247
-
H.-P. Wessel, T. Iversen, D. R. Bundle, J. Chem. Soc., Perkin Trans. 1 1985, 2247. doi:10.1039/P19850002247
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J. Chem. Soc., Perkin Trans. 1
, pp. 2247
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Wessel, H.-P.1
Iversen, T.2
Bundle, D.R.3
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23
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33748223304
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-
doi:10.1002/ANIE.199005141
-
U. Schmidt, A. Lieberknecht, U. Kazmaier, E. Haslinger, Angew. Chem. Int. Ed. Engl. 1990, 29, 514. doi:10.1002/ANIE.199005141
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, vol.29
, pp. 514
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-
Schmidt, U.1
Lieberknecht, A.2
Kazmaier, U.3
Haslinger, E.4
-
24
-
-
49749113207
-
-
Although Scheme 8 depicts the Z-dehydro compound 58, no attempt was made to determine the double bond configuration
-
Although Scheme 8 depicts the Z-dehydro compound 58, no attempt was made to determine the double bond configuration.
-
-
-
-
25
-
-
49749140327
-
-
K. Okamoto, H. Abe, K. Kuromizu, N. Izumiya, Mem. Fac. Sci. Kyushu Ser. C 1914, 9, 131.
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, vol.9
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Okamoto, K.1
Abe, H.2
Kuromizu, K.3
Izumiya, N.4
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28
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0002714675
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doi:10.1021/JO00408A041
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W. C. Still, M. Kahn, A. Mitra, J. Org. Chem. 1978, 43, 2923. doi:10.1021/JO00408A041
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J. Org. Chem
, vol.43
, pp. 2923
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Still, W.C.1
Kahn, M.2
Mitra, A.3
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