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rhodium asymmetric hydrogenation enamide dehydroamino acid DIPAMP BINAPINE SEGPHOS chiral ruthenium BINAP diamine aryl ketone DPEN DAIPEN Noyori asymmetric transfer hydrogenation TsDPEN ketone reduction palladium asymmetric cross-coupling Suzuki Heck atroposelective ketone CBS oxazaborolidine borane Corey copper conjugate addition 1,4-addition quaternary center phosphoramidite BOX chiral phosphoric acid TRIP BINOL organocatalysis Brønsted acid titanium TADDOL Lewis acid Diels-Alder carbonyl-ene cyanation metathesis Grubbs Hoveyda-Grubbs ring-closing cross-metathesis manganese Mn-salen Jacobsen base metal epoxidation pincer Buchwald biaryl phosphine SPhos XPhos RuPhos iridium unfunctionalized olefin MonoPhos Crabtree NHC IMes IPr carbene Trost DACH allylic alkylation API nickel Negishi spiro SPINOL SIPHOS Zhou Qi-Lin rigid backbone iron cobalt sustainable hydroformylation Xantphos Biphephos oxo process industrial C-H activation directing group olefin hydroboration hydrosilylation MacMillan imidazolidinone SOMO photoredox dual catalysis radical visible light cinchona alkaloid phase-transfer cinchonidine quinine Jorgensen Hayashi diarylprolinol enamine iminium BINAL-H chiral hydride reduction bisoxazoline cycloaddition t-Bu-BOX DIOP hydrogenation bisphosphine CHIRAPHOS PROPHOS evolution allylic substitution green chemistry flow chemistry ionic liquids proline DMAP sustainability process catalysis custom synthesis CDMO manufacturing

Rigid Backbone

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Spiro Bisphosphine Ligands: SPINOL and SIPHOS in Asymmetric Catalysis

Chiral spiro ligands, developed primarily by Zhou Qi-Lin and coworkers at Nankai University, occupy a distinctive position in the ligand landscape. Their defining feature is a …

2026-04-22
Methodology, Science 6 tags
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