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| - article (en)
- wetenschappelijk artikel (nl)
- наукова стаття, опублікована в липні 2000 (uk)
- article scientifique publié en 2000 (fr)
- im Juli 2000 veröffentlichter wissenschaftlicher Artikel (de)
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| - Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie (en)
- Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie (nl)
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| - Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie (en)
- Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie (nl)
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| - Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie (en)
- Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie (nl)
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| - Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie ed Applicazioni", and the University of Bologna (funds for selected research topics) for financial support of this research (en)
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| - 10.1002/1521-3773(20000703)39:13<2327::AID-ANIE2327>3.0.CO;2-9
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of | - Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation
- Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency
- anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents
- Catalytic enantioselective Grignard Nozaki-Hiyama methallylation from the alcohol oxidation level: chloride compensates for π-complex instability
- Diastereo- and enantioselective ruthenium-catalyzed hydrohydroxyalkylation of 2-silyl-butadienes: carbonyl syn-crotylation from the alcohol oxidation level
- Unprecedented detection of inherent chirality in uranyl-salophen complexes
- (2Z,2'Z,4E,4'E)-4,4'-(Cyclo-hexane-1,2-diyldinitrilo)dipent-2-en-2-ol
- Two Novel Vanadium Tellurites Covalently Bonded with Metal−Organic Complex Moieties: M(phen)V2TeO8 (M = Cu, Ni)
- Hydrothermal syntheses, crystal structures, and magnetic properties of inorganic-organic hybrid vanadium selenites with zero- to three-dimensional structures: (1,10-phenanthroline)(2)V(2)SeO(7), (2,2'-bipyridine)VSeO(4), (4,4'-bipyridine)V(2)Se(2)O(
- (1Z,1'Z,3E,3'E)-1,1'-Diphenyl-3,3'-[(1S,2S)-cyclo-hexane-1,2-diyldinitrilo]dibut-1-en-1-ol
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