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For Rh-catalyzed hydrogenation of unsaturated acids see and Refs. 4a,b
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-
22
-
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47749089043
-
-
note
-
Synthesis of substrate 1 will be reported elsewhere.
-
-
-
-
23
-
-
47749088293
-
-
note
-
n] led to full conversions and less than 25% ee's.
-
-
-
-
24
-
-
47749095084
-
-
note
-
See Supplementary data for bisphosphine ligands employed in the initial catalyst testing.
-
-
-
-
25
-
-
47749108362
-
-
note
-
Conversions and ee's throughout this study were determined by HPLC analysis using Chiracel AD-H column, hexane/i-PrOH = 80:20, after conversion to methyl ester.
-
-
-
-
26
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0030790831
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Rossen K., Pye P.J., Reamer R.A., Tsou N.N., Volante R.P., and Reider P.J. J. Am. Chem. Soc. 119 (1997) 6207
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29
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Pye P.J., Rossen K., Reamer R.A., Volante R.P., and Reider P.J. Tetrahedron Lett. 39 (1998) 4441
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32
-
-
47749093959
-
-
note
-
Solvent screening at S/C 500, 10 bar, 40 °C showed early on that MeOH was the best solvent for use in this system.
-
-
-
-
35
-
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0037708568
-
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Ashcroft C.P., Challenger S., Derrik A.M., Storey R., and Thomson N.M. Org. Proc. Res. Dev. 7 (2003) 362
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Storey, R.4
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-
37
-
-
47749090577
-
-
note
-
n] catalyst.
-
-
-
-
38
-
-
47749104181
-
-
note
-
3N as an additive, no conversion was observed in this system.
-
-
-
-
39
-
-
47749129692
-
-
note
-
2O in such systems led to low conversions and partial deprotection of the Boc group (3-15%).
-
-
-
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