Title : Employing the structural diversity of nature: development of modular dipeptide-analogue ligands for ruthenium-catalyzed enantioselective transfer hydrogenation of ketones.

Pub. Date : 2003 Sep 5

PMID : 12953189






3 Functional Relationships(s)
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Protein Name
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1 The combination N-Boc-L-alanine and (R)-phenylglycinol (Boc-L-Ab) or its enantiomer (N-Boc-D-alanine and (S)-phenylglycinol, Boc-D-Aa) proved to be the best ligands for the reduction process. 2-amino-2-phenylethanol BOC cell adhesion associated, oncogene regulated Homo sapiens
2 The combination N-Boc-L-alanine and (R)-phenylglycinol (Boc-L-Ab) or its enantiomer (N-Boc-D-alanine and (S)-phenylglycinol, Boc-D-Aa) proved to be the best ligands for the reduction process. 2-amino-2-phenylethanol BOC cell adhesion associated, oncogene regulated Homo sapiens
3 The combination N-Boc-L-alanine and (R)-phenylglycinol (Boc-L-Ab) or its enantiomer (N-Boc-D-alanine and (S)-phenylglycinol, Boc-D-Aa) proved to be the best ligands for the reduction process. 2-amino-2-phenylethanol BOC cell adhesion associated, oncogene regulated Homo sapiens