about
Isocyanide-Based Multicomponent Reactions for the Synthesis of HeterocyclesIdentification of Novel Epoxide Inhibitors of Hepatitis C Virus Replication Using a High-Throughput ScreenThree-component asymmetric catalytic Ugi reaction--concinnity from diversity by substrate-mediated catalyst assembly.Multicomponent reaction design in the quest for molecular complexity and diversity.Palladium-catalyzed chemoselective synthesis of indane-1,3-dione derivatives via tert-butyl isocyanide insertion.Asymmetric multicomponent reactions (AMCRs): the new frontier.Enantioselective synthesis of α-oxy amides via Umpolung amide synthesisAsymmetric synthesis of diverse glycolic acid scaffolds via dynamic kinetic resolution of α-keto estersChemistry and biology of multicomponent reactions.Recent developments in asymmetric multicomponent reactions.Efficient synthesis of boron-containing α-acyloxyamide analogs via microwave irradiation.Enantioselective organocatalytic Hantzsch synthesis of polyhydroquinolines.Stereoselective Synthesis of Functionalized Bicyclic Scaffolds by Passerini 3-Center-2-Component Reactions of Cyclic Ketoacids.Studies on the chemistry and reactivity of alpha-substituted ketones in isonitrile-based multicomponent reactionsZeolite catalyzed solvent-free one-pot synthesis of dihydropyrimidin-2(1H)-ones--a practical synthesis of monastrol.An Efficient Nickel-Catalyzed Asymmetric Oxazole-Forming Ugi-Type Reaction for the Synthesis of Chiral Aryl-Substituted THIQ Rings.Chiral Phosphoric Acid Catalyzed Asymmetric Ugi Reaction by Dynamic Kinetic Resolution of the Primary Multicomponent Adduct.Carboxylic acid free novel isocyanide-based reactions.
P2860
Q26772038-1FD31335-8C4C-48A7-9C11-46E4D2A6E1FDQ27481404-2CCF5A7F-A73B-42B3-89F5-CE4895649CF8Q33566408-40B21B44-4644-4229-B810-8493FEA23C15Q33944558-C4A8BB04-C815-4DE2-B90D-16C78BA6E154Q35640706-7AE965CC-7747-4149-AAA7-1AD1F2D8C6A0Q36047385-EACBDF2D-D1E5-4EF2-BD59-45130B14945CQ36337558-574BA338-11E2-4D7A-906D-3A8F3CB1B05CQ36497437-A405A50F-D6EC-4F3B-BA1F-13ABEA318A8CQ37017587-350C71C1-C4E6-42EC-91E0-1F6B2B3C35BAQ38006603-ED7A9B21-EE02-4B67-B7B9-A3758EEFC28DQ39107032-46C3082C-6A42-4FD2-9FF6-3E2732C04088Q42020567-082B0DD1-026F-4503-AFD4-1DF33E9B6E77Q42267047-A6C8DE2A-5C98-4C9A-971B-81259FC99D0EQ42542518-7661CA0B-1D8A-4DD0-8B3D-5D6FE44CB4B7Q43171438-00A7EB0B-E3AD-4B80-B9FD-2A4341D745C6Q48193699-C33F1BAC-6CE2-4793-938D-F47EB151FC99Q51430769-2CCE5024-7DA1-4845-8E55-E855DF62F7A0Q51757254-5DA3FF1E-EF1B-4CD4-8B17-AAA777E89BE3
P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Stereochemical control of the Passerini reaction
@en
Stereochemical control of the Passerini reaction
@nl
type
label
Stereochemical control of the Passerini reaction
@en
Stereochemical control of the Passerini reaction
@nl
prefLabel
Stereochemical control of the Passerini reaction
@en
Stereochemical control of the Passerini reaction
@nl
P2093
P2860
P356
P1433
P1476
Stereochemical control of the Passerini reaction
@en
P2093
Chang C Liu
Peter R Andreana
Stuart L Schreiber
P2860
P304
P356
10.1021/OL0482893
P407
P577
2004-11-01T00:00:00Z