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3
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Oishi, T.1
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8
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f) H. Oguri, S. Hishiyama, O. Sato, T. Oishi, M. Hirama, M. Murata, T. Yasumoto, and N. Harada, Tetrahedron, 53, 3057 (1997).
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Murata, M.6
Yasumoto, T.7
Harada, N.8
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9
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0027751677
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a) M. Sasaki, A. Hasegawa, and K. Tachibana, Tetrahedron Lett., 34, 8489 (1993);
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Sasaki, M.1
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Tachibana, K.3
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10
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0040753562
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submitted
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M. Satake, A. Morohashi, H. Oguri, T. Oishi, M. Hirama, N. Harada, and T. Yasumoto, to be submitted.
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Satake, M.1
Morohashi, A.2
Oguri, H.3
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Harada, N.6
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13
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15
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b) T. Oishi, K. Iida, and M. Hirama, Tetrahedron Lett., 34, 3573 (1993).
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16
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33847799798
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R. E. Ireland, R. H. Mueller, and A. K. Willard, J. Am. Chem. Soc., 98, 2868 (1976).
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Ireland, R.E.1
Mueller, R.H.2
Willard, A.K.3
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17
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33947469257
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The stereochemistry was determined by conversion of 5 into (S,S)-2,3-dimethylbutane-1,4-diol: G. E. McCasland and S. Proskow, J. Am. Chem. Soc., 78, 5646 (1956).
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McCasland, G.E.1
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19
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0040159405
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note
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Intermediary of epoxide was supported by isolation without the subsequent acid treatment.
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20
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0040159406
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note
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The stereochemistry of 7, 9, and 10 was determined by NOE experiments. (formula presented)
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21
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0024840703
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E. J. Corey, P. D. Jardine, S. Virgil, P.-W. Yuen, and R. D. Connell J. Am. Chem. Soc., 111, 9243 (1989).
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Connell, R.D.5
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22
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0021775497
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S. Masamune, W. Choy, J. S. Petersen, and L. R. Sita, Angew. Chem., Int. Ed. Engl. 24, 1 (1985).
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Masamune, S.1
Choy, W.2
Petersen, J.S.3
Sita, L.R.4
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23
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0038975186
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ref. 2c
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The stereoselectivity due to substrate control appears to vary with the size of reagent. Related phenomena have been observed: see ref. 2c and T. Oishi, T. Iwakuma, M. Hirama, and S. Itô, Synlett, 1995, 404.
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Synlett
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Oishi, T.1
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Hirama, M.3
Itô, S.4
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24
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0038975188
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note
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3) δ 13.65, 15.87, 40.56, 41.87, 45.68, 61.96, 70.68, 71.94, 74.40, 109.21, (TIPS group was omitted).
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