Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.4.16.2 (PCP)
3,761 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A range of chiral resorcinol bis(phosphite) and phosphite-phosphinite ligands were produced and their propensity to form palladium PCP-pincer complexes examined. The ease of base-assisted C-H palladation of the ligands falls in the order bis(phosphinite) > phosphite-phosphinite > bis(phosphite). The catalytic activity of the complexes in the asymmetric allylation of benzaldehyde with allyl tributyltin was examined and it was found that, contrary to expectations, ligands with 3,3'-disubstituted BINOL residues show poorer activity and stereoselectivity than unsubstituted BINOL analogues. In addition the order of activity of the pincer complexes was established as bis(phosphite) > phosphite-phosphinite > bis(phosphinite). Crystal structures of representative examples of a 3,3'-disubstituted BINOL, mono- and bis(phosphite) ligands based on 2,4-di-tert-butyl resorcinol and Pd complexes of two of the chiral complexes are presented.
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PMID:Tuning ligand structure in chiral bis(phosphite) and mixed phosphite-phosphinite PCP-palladium pincer complexes. 2181 90

The synthesis of macrocyclic variants of commonly employed phosphine-based pincer (pro)ligands derived from meta-xylene (PCP-14) and resorcinol (POCOP-14) is described, where the P-donors are trans-substituted with a tetradecamethylene linker. The former was accomplished using a seven-step asymmetric procedure involving (-)-cis-1-amino-2-indanol as a chiral auxiliary and ring-closing olefin metathesis. A related, but non-diastereoselective route was employed for the latter, which consequently necessitated chromatographic separation from the cis-substituted by-product. The proligands are readily metalated and homologous series of MI(CO) and MIIICl2(CO) derivatives (M = Rh, Ir) have been isolated and fully characterised in solution and the solid state. Metal hydride complexes are generated during the synthesis of the former and have been characterised in situ using NMR spectroscopy.
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PMID:Synthesis and group 9 complexes of macrocyclic PCP and POCOP pincer ligands. 3203 Nov 94