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0345611266
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note
-
Both enantiomers of 3 were converted into the corresponding methyl esters (S)- and (R)-2. The determination of their enantiomeric purity was performed with chiral HPLC on tris(3,5-dimethylphenyl)carbamate derivative of cellulose in Prof. F. Vögtle's laboratory (see Acknowledgements).
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-
-
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20
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84985668694
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21
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84981800009
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2 as a reagent was reported earlier: (a) Falk, H.; Schlogl, K. Angew. Chem., Int. Ed. Engl. 1968, 7, 383; (b) Falk, H.; Reich-Rohrwig, P.; Schlogl, K. Tetrahedron 1970, 26, 511; (c) The synthesis of ketone 1 by the reaction of acid 3 with methyllithium as a reagent with 54% chemical yield was also described with reference to 14(b) but without any experimental details or synthetic technique disclosed, Delton, M. J.; Cram, D. J. J. Am. Chem. Soc. 1972, 94, 2471.
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Falk, H.1
Schlogl, K.2
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22
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0000018043
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2 as a reagent was reported earlier: (a) Falk, H.; Schlogl, K. Angew. Chem., Int. Ed. Engl. 1968, 7, 383; (b) Falk, H.; Reich-Rohrwig, P.; Schlogl, K. Tetrahedron 1970, 26, 511; (c) The synthesis of ketone 1 by the reaction of acid 3 with methyllithium as a reagent with 54% chemical yield was also described with reference to 14(b) but without any experimental details or synthetic technique disclosed, Delton, M. J.; Cram, D. J. J. Am. Chem. Soc. 1972, 94, 2471.
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Falk, H.1
Reich-Rohrwig, P.2
Schlogl, K.3
-
23
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0013398257
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2 as a reagent was reported earlier: (a) Falk, H.; Schlogl, K. Angew. Chem., Int. Ed. Engl. 1968, 7, 383; (b) Falk, H.; Reich-Rohrwig, P.; Schlogl, K. Tetrahedron 1970, 26, 511; (c) The synthesis of ketone 1 by the reaction of acid 3 with methyllithium as a reagent with 54% chemical yield was also described with reference to 14(b) but without any experimental details or synthetic technique disclosed, Delton, M. J.; Cram, D. J. J. Am. Chem. Soc. 1972, 94, 2471.
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Delton, M.J.1
Cram, D.J.2
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27
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0344749168
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Canadian Patent 638.335 (1962)
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(b) Gorham, W. F. Canadian Patent 638.335 (1962).
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Gorham, W.F.1
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