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36
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29344456801
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note
-
8 Their success might be attributed to an indirect tactics in the construction of the C5 stereogenic center via aldol coupling .with aldehyde followed by oxidation and diastereoselective addition of vinylmagnesium bromide as the latent carboxyl functionality.
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-
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37
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85086526049
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note
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5c
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39
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84985534941
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Naef, R.; Seebach, D. Angew. Chem., Int. Ed. Engl. 1981, 20, 1030.
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42
-
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85086526421
-
-
note
-
2-mediated aldol coupling was not explored. In this regard, it is also worthy of note that neither of the corresponding silyl ketene acetals proved to be stable enough to be prepared.
-
-
-
-
43
-
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29344467000
-
-
note
-
3 and methine proton in 10, whereas the corresponding signal enhancement was not observed with 11.
-
-
-
-
45
-
-
85086525890
-
-
note
-
2S.
-
-
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46
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33845184924
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Angelastro, M. R.; Peet, N. P.; Bey, P. J. Org. Chem. 1989, 54, 3913.
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-
47
-
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85086526013
-
-
note
-
4 were found to be effective for the present aldol coupling.
-
-
-
-
48
-
-
85086526408
-
-
note
-
1H NMR signals for the S-methyl protons, which were always 0.04-0.1 ppm downfield in the desired product relative to its C5 epimer.
-
-
-
-
49
-
-
85086528306
-
-
note
-
23 failed, simply because the reaction did not work.
-
-
-
-
50
-
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1542545591
-
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Trost, B. M., Ed.; Blackwell Scientific Publications: Oxford
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Mukaiyama, T.; Kobayashi, S. In Stereocontrolled Organic Synthesis, Trost, B. M., Ed.; Blackwell Scientific Publications: Oxford, 1994; p 37.
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Mukaiyama, T.1
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0016591075
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Masamune, S.; Kamata, S.; Schilling, W. J. Am. Chem. Soc. 1975, 97, 3515.
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53
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29344451269
-
-
note
-
The synthesis of alkyne 36 will be reported in a full account.
-
-
-
-
55
-
-
85086526868
-
-
note
-
2)].
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-
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