Phosphine-catalyzed enantioselective intramolecular [3+2] annulations to generate fused ring systems.
about
Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis.Nucleophilic Chiral Phosphines: Powerful and Versatile Catalysts for Asymmetric AnnulationsRapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow-Generated Diazo Compounds and Propargylated AminesEnantioselective Synthesis of Isoquinolines: Merging Chiral-Phosphine and Gold Catalysis.From Mechanistic Study to Chiral Catalyst Optimization: Theoretical Insight into Binaphthophosphepine-catalyzed Asymmetric Intramolecular [3 + 2] Cycloaddition.Chiral phosphine-mediated intramolecular [3 + 2] annulation: enhanced enantioselectivity by achiral Brønsted acid.Harnessing sunlight without a photosensitizer for highly efficient consecutive [3+2]/[4+2] annulation to synthesize fused benzobicyclic skeletons.Ferrocene Derived Bifunctional Phosphine-Catalyzed Asymmetric Oxa-[4+2] Cycloaddition of α-Substituted Allenones with Enones.Engaging Allene-Derived Zwitterions in an Unprecedented Mode of Asymmetric [3+2]-Annulation Reaction.Multifunctional chiral phosphine-catalyzed [3+2] annulation of Morita-Baylis-Hillman carbonates with cyclopentenones: asymmetric synthesis of 4-oxo-hexahydropentalenes.Phosphine-Catalyzed β,γ-Umpolung Domino Reaction of Allenic Esters: Facile Synthesis of Tetrahydrobenzofuranones Bearing a Chiral Tetrasubstituted Stereogenic Carbon Center.Phosphine-catalyzed [5+1] annulation of δ-sulfonamido-substituted enones with N-sulfonylimines: a facile synthesis of tetrahydropyridines.Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones.Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow-Generated Diazo Compounds and Propargylated Amines
P2860
Q37263721-49934410-42CB-4BC8-87CD-A4B6F01B305EQ37574112-D26A162E-7C18-46A5-AF73-DA6199110D13Q37717812-533D0ADE-EA1A-407A-87E6-46299CE20DDEQ38779609-53990781-6F02-462B-A6AB-28C50E52BB4CQ41309023-83F82ADD-804E-4C1A-A867-AE41569A913FQ42365778-98F4D907-C1D1-48D4-B089-57298DBD3958Q47671813-539880DF-06DC-4DCA-9E75-05052CFF1D66Q47763290-973E4177-1AAF-45A3-8F96-069D6AE70BE5Q48185162-364CCC80-8E91-49EF-8A96-8C58253EBA49Q49899915-C91C621E-6D50-405F-985C-BA534287681BQ51658792-99F535D0-34A0-4BB5-ABEF-69D9AC90D34AQ52575905-EB173B25-0056-4C0D-9DD0-04CE4BFE9E2DQ54637181-7CD9457B-4337-4259-90D6-E244EEA77954Q55112417-22DC06C8-8904-4482-967A-C01074C252A0Q56951369-CC1C3568-620B-4888-A1A0-7412DD320A67
P2860
Phosphine-catalyzed enantioselective intramolecular [3+2] annulations to generate fused ring systems.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@ast
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@en
type
label
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@ast
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@en
prefLabel
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@ast
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@en
P2093
P2860
P356
P1476
Phosphine-catalyzed enantiosel ...... o generate fused ring systems.
@en
P2093
Atsuko Nishiguchi
Gregory C Fu
Sarah Yunmi Lee
Yuji Fujiwara
P2860
P304
P356
10.1021/JACS.5B01985
P407
P50
P577
2015-03-27T00:00:00Z