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Combinatorial Chemistry for Ligand Development in Catalysis: Synthesis and Catalysis Screening of Peptidosulfonamide Tweezers on the Solid Phase
On the basis of a pyrrolidine tweezer 1, a library of peptidosulfonamide tweezers (15a−e, 16a−e) was synthesized on the solid phase. This library was screened in a simultaneous substrate screening procedure for the ability to enantioselectively catalyze the Ti(O-i-Pr)4-mediated addition of diethylzi...
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Published in: | Journal of organic chemistry 2000-03, Vol.65 (6), p.1750-1757 |
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Language: | English |
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container_end_page | 1757 |
container_issue | 6 |
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container_title | Journal of organic chemistry |
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creator | Brouwer, Arwin J van der Linden, Heiko J Liskamp, Rob M. J |
description | On the basis of a pyrrolidine tweezer 1, a library of peptidosulfonamide tweezers (15a−e, 16a−e) was synthesized on the solid phase. This library was screened in a simultaneous substrate screening procedure for the ability to enantioselectively catalyze the Ti(O-i-Pr)4-mediated addition of diethylzinc to aldehydes. One of the best solid-phase tweezer catalyst (i.e., 16d, giving an ee of 32% in solid-phase catalysis) was resynthesized in solution (compounds 20 and 21). The now homogeneous solution-phase catalysis showed even better enantioselectivity (i.e., up to 66%). |
doi_str_mv | 10.1021/jo991628z |
format | article |
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title | Combinatorial Chemistry for Ligand Development in Catalysis: Synthesis and Catalysis Screening of Peptidosulfonamide Tweezers on the Solid Phase |
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