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0001525655
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0344954128
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17
-
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0344523286
-
-
note
-
4
-
-
-
-
18
-
-
0345385595
-
-
note
-
4 gave 8 without decreasing the yield, and 8 was isolated at this stage. Thus, the somewhat tedious MPLC separation of 3 and 4 can be avoided.
-
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-
-
21
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-
0001060253
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(b) Baldwin, J. E.; Adlington, R. M.; Rawlings, B. Tetrahedron Lett. 1985, 26, 481.
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0030944661
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Godier-Marc, E.1
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0029101362
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(b) Wick, L.; Tamm, C.; Boller, T. Helv. Chim. Acta 1995, 78, 403.
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0038459459
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Jiménez, J.M.1
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Ortuno, R.M.3
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26
-
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0001217562
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(d) A single stereoisomer (12% yield) without assignment of stereochemistry. Horikawa, H.; Nishitani, T.; Iwasaki, T.; Inoue, I. Tetrahedron Lett. 1983, 24, 2193.
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2542433188
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Sharpless, K.B.4
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28
-
-
0344092130
-
-
note
-
The reaction can be carried out using crude 7, which was prepared from the mixture of cyclopropane 3 and cyclobutane 4 without separation, and was purified from the small amount of impurity arising from 4 at this stage. See also ref 8.
-
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29
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35848945419
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-
-
0344523283
-
-
note
-
3, and cyclopropyl carbons were observed for Boc-protected ACCs, 12, 17, and 21.
-
-
-
-
32
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0030733658
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Hibbs, D. E.; Hursthouse, M. B.; Jones, I. G.; Jones, W.; Malik, K. M. A.; North, M. Tetrahedron, 1997, 53, 17417.
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Jones, W.4
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North, M.6
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