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2 (60 μL).
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This calculation is further clarified by Scheme 1 in the Supporting Information.
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Mannschreck, A.4
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84982376647
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(e) Simon, H.; Rambeck, B.; Hashimoto, H.; Günther, H.; Nohynek, G. ; Neumann, H. Angew. Chem., Int. Ed. 1974, 13, 608.
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Simon, H.1
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Hashimoto, H.3
Günther, H.4
Nohynek, G.5
Neumann, H.6
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76
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2342572162
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note
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2H NMR spectrum of 2- and 3-phenylpropanal-derived (S)-methyl mandelate esters gave 65.7% (R,S)-5 and 34.3% (S,S)-5.
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77
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0033521183
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(a) Lenges, C. P.; Brookhart, M. Angew. Chem., Int. Ed. 1999, 38, 3533.
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(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 3533
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Lenges, C.P.1
Brookhart, M.2
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78
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0032558084
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(b) Brookhart, M.; Lenges, C. P.; White, P. S. J. Am. Chem. Soc. 1999, 120, 6965.
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(1999)
J. Am. Chem. Soc.
, vol.120
, pp. 6965
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Brookhart, M.1
Lenges, C.P.2
White, P.S.3
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79
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0025272121
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(c) Kondo, T.; Akazome, Y.; Tsuij, Y.; Watanabe, Y. J. Org. Chem. 1990, 55, 1286.
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(1990)
J. Org. Chem.
, vol.55
, pp. 1286
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Kondo, T.1
Akazome, Y.2
Tsuij, Y.3
Watanabe, Y.4
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80
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2342536300
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note
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+ 134 (44.78)].
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81
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2342512718
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note
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2 pressure. The formula for calculating the ratio of R-acyl cleavage t S-acyl cleavage is: (8y x 9) = (13 x 32) where y = 5.8, the rate at which the R-acyl is cleaved as compared to cleavage of the S-acyl.
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