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13
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0007397552
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and references cited therein
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Harada, N.1
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Kuriki, T.4
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Swarts, H.J.2
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De Groot, A.4
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15
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0343131308
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In fact, we have synthesized (-)-1 from (-)-Wieland-Mischer ketone using the procedure described by Paquette for (+)-1
-
In fact, we have synthesized (-)-1 from (-)-Wieland-Mischer ketone using the procedure described by Paquette for (+)-1.
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16
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0002900717
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Rinderknecht, B. L.; Gloer, J. B.; Dowd, P. F.; Wicclow, D. T. J. Org. Chem. 1989, 54, 2530-2532.
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0030010207
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Teranaka, M.3
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19
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0031760185
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Iwagawa, T.; Kaneko, M.; Okamura, H.; Nakatani, M.; van Soest, R. W. M. J. Nat. Prod. 1998, 61, 1310-1312.
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Iwagawa, T.1
Kaneko, M.2
Okamura, H.3
Nakatani, M.4
Van Soest, R.W.M.5
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20
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0344003475
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-
21
-
-
0343567196
-
-
Note
-
21 (50% for the two steps) and further formylation and treatment with N-methylaniline (77% for the two steps, operating in a 0.22 mol scale). The overall yield is lower than that obtained from (R)-3-methylcyclohexanone and the sequence involves four steps, instead of the three required in the route depicted in .
-
-
-
-
22
-
-
0009822575
-
-
Lee, R. A.; McAndrews, C.; Patel, K. M.; Reusch, W. Tetrahedron Lett. 1973, 965-968.
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Lee, R.A.1
McAndrews, C.2
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Reusch, W.4
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23
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37049075427
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Tori, M.1
Uchida, N.2
Sumida, A.3
Furuta, H.4
Asakawa, Y.5
-
24
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-
0033548371
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-
For an enantioselective synthesis of the corresponding methyl ester, which appeared when the work had been done, see:
-
For an enantioselective synthesis of the corresponding methyl ester, which appeared when the work had been done, see: Tori, M.; Hisazumi, K.; Wada, T.; Sono, M.; Nakashima, K. Tetrahedron: Asymmetry 1999, 10, 961-971.
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Tetrahedron: Asymmetry
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, pp. 961-971
-
-
Tori, M.1
Hisazumi, K.2
Wada, T.3
Sono, M.4
Nakashima, K.5
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25
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0344003471
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-
We acknowledge a reviewer's suggestions concerning this question
-
We acknowledge a reviewer's suggestions concerning this question.
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