Total synthesis and isolation of citrinalin and cyclopiamine congeners.
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Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product SynthesisCycloexpansamines A and B: spiroindolinone alkaloids from a marine isolate of Penicillium sp. (SF-5292).Catalyst control over regio- and enantioselectivity in Baeyer-Villiger oxidations of functionalized ketonesMitragynine/Corynantheidine Pseudoindoxyls As Opioid Analgesics with Mu Agonism and Delta Antagonism, Which Do Not Recruit β-Arrestin-2.Squaramide-Catalyzed Synthesis of Enantioenriched Spirocyclic Oxindoles via Ketimine Intermediates with Multiple Active Sites.Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.Synthesis of Structurally Diverse 2,3-Fused Indoles via Microwave-Assisted AgSbF6-Catalysed Intramolecular Difunctionalization of o-AlkynylanilinesA diversity-oriented approach to indolocarbazoles via Fischer indolization and olefin metathesis: total synthesis of tjipanazole D and I.Sclerotiamide: The First Non-Peptide-Based Natural Product Activator of Bacterial Caseinolytic Protease P.Terpenoid biosynthesis off the beaten track: unconventional cyclases and their impact on biomimetic synthesis.Synthetic approaches towards alkaloids bearing α-tertiary amines.Computational Chemistry to the Rescue: Modern Toolboxes for the Assignment of Complex Molecules by GIAO NMR Calculations.Applications of Nonenzymatic Catalysts to the Alteration of Natural Products.Total Synthesis and Structural Reassignment of Aspergillomarasmine A.Construction of highly enantioenriched spirocyclopentaneoxindoles containing four consecutive stereocenters via thiourea-catalyzed asymmetric Michael-Henry cascade reactions.Biosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E, leuconolam, and rhazinilam.Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.Total synthesis of aspeverin via an iodine(III)-mediated oxidative cyclization.Total Synthesis of Notoamides F, I, and R and Sclerotiamide.Nine-step total synthesis of (-)-strychnofoline.One-pot green synthesis of biologically relevant novel spiro[indolin-2-one-3,4'-pyrano[2,3-c]pyrazoles] and studies on their spectral and X-ray crystallographic behaviors.Stereoselective Synthesis of Polycycles Containing an Aziridine Group: Intramolecular aza-Diels-Alder Reactions of Unactivated 2H-Azirines with Unactivated Dienes.An unusual stereoretentive 1,3-quaternary carbon shift resulting in an enantioselective RhII-catalyzed formal [4+1]-cycloaddition between diazo compounds and vinyl ketenes.One-pot and Environmentally Friendly Synthesis of New Spiroindolones Using Functionalized Multiwall Carbon Nanotubes as Powerful Catalyst
P2860
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P2860
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
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
name
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@ast
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@en
type
label
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@ast
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@en
prefLabel
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@ast
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@en
P2093
P2860
P356
P1433
P1476
Total synthesis and isolation of citrinalin and cyclopiamine congeners.
@en
P2093
David E Williams
Dean J Tantillo
Eduardo V Mercado-Marin
Eli F Pimenta
Michael W Lodewyk
Pablo Garcia-Reynaga
Raymond J Andersen
Richmond Sarpong
Roberto G S Berlinck
Stelamar Romminger
P2860
P2888
P304
P356
10.1038/NATURE13273
P407
P577
2014-05-01T00:00:00Z
P5875
P6179
1000345642