about
Total synthesis of vinblastine, related natural products, and key analogues and development of inspired methodology suitable for the systematic study of their structure-function propertiesOrganic chemistry. Practical olefin hydroamination with nitroarenesRadicals: Reactive Intermediates with Translational PotentialNickel-catalysed retro-hydroamidocarbonylation of aliphatic amides to olefinsFunctionalized olefin cross-coupling to construct carbon-carbon bonds.Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives.Total Synthesis of (-)-Vindoline and (+)-4-epi-Vindoline Based on a 1,3,4-Oxadiazole Tandem Intramolecular [4 + 2]/[3 + 2] Cycloaddition Cascade Initiated by an Allene Dienophile.Fragment Coupling and the Construction of Quaternary Carbons Using Tertiary Radicals Generated From tert-Alkyl N-Phthalimidoyl Oxalates By Visible-Light PhotocatalysisTandem Intramolecular Diels-Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Initial Scope and Applications.Practical carbon-carbon bond formation from olefins through nickel-catalyzed reductive olefin hydrocarbonation.Recent advances in the synthesis of natural multifunctionalized decalins.Catalysis of Radical Reactions: A Radical Chemistry Perspective.Markovnikov free radical addition reactions, a sleeping beauty kissed to life.Shuttle Catalysis-New Strategies in Organic Synthesis.Mn-, Fe-, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins.Proton-Coupled Electron Transfer in Organic Synthesis: Fundamentals, Applications, and Opportunities.Synthesis and Fungicidal Activities of (Z/E)-3,7-Dimethyl-2,6-octadienamide and Its 6,7-Epoxy Analogues.Ph(i-PrO)SiH2: An Exceptional Reductant for Metal-Catalyzed Hydrogen Atom Transfers.Hydromethylation of Unactivated Olefins.Simple, chemoselective, catalytic olefin isomerizationIndole diterpenoid natural products as the inspiration for new synthetic methods and strategiesFour-step synthesis of the antimalarial cardamom peroxide via an oxygen stitching strategy.Redox-triggered C-C coupling of alcohols and vinyl epoxides: diastereo- and enantioselective formation of all-carbon quaternary centers via tert-(hydroxy)-prenylation.Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling.Fe-Catalyzed C-C Bond Construction from Olefins via Radicals.Development of a concise synthesis of ouabagenin and hydroxylated corticosteroid analogues.Arenophile-Mediated Dearomative Reduction.Wacker-Type Oxidation Using an Iron Catalyst and Ambient Air: Application to Late-Stage Oxidation of Complex Molecules.Asymmetric Total Synthesis of Hispidanin A.Radical Cyclization of Alkene-Tethered Ketones Initiated by Hydrogen-Atom Transfer.First-Row Late Transition Metals for Catalytic Alkene Hydrofunctionalisation: Recent Advances in C-N, C-O and C-P Bond Formation.Total synthesis of complex terpenoids employing radical cascade processes.Synthesis of stilbene derivatives via visible-light-induced cross-coupling of aryl diazonium salts with nitroalkenes using -NO2 as a leaving group.Catalytic reversible alkene-nitrile interconversion through controllable transfer hydrocyanation.Scalable Total Synthesis of rac-Jungermannenones B and C.Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies.Atom-economical cobalt-catalysed regioselective coupling of epoxides and aziridines with alkenes.Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol.Enantioselective synthesis of Iboga alkaloids and vinblastine via rearrangements of quaternary ammoniums† †Electronic supplementary information (ESI) available: Experimental procedures and characterisation data for all compounds are provided. CCDC 1Synthesis and Study of the Antimalarial Cardamom Peroxide
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P2860
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
A practical and catalytic reductive olefin coupling.
@en
type
label
A practical and catalytic reductive olefin coupling.
@en
prefLabel
A practical and catalytic reductive olefin coupling.
@en
P2093
P2860
P356
P1476
A practical and catalytic reductive olefin coupling.
@en
P2093
Julian C Lo
Phil S Baran
P2860
P304
P356
10.1021/JA4117632
P407
P577
2014-01-15T00:00:00Z