Total synthesis and isolation of citrinalin and cyclopiamine congeners. - Wikidata - wikimedia - TriplyDB

Total synthesis and isolation of citrinalin and cyclopiamine congeners.

Total synthesis and isolation of citrinalin and cyclopiamine congeners.

http://www.wikidata.org/entity/Q33980370

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Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product Synthesis Cycloexpansamines 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 ketones Mitragynine/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-Alkynylanilines A 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

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P2860

Total synthesis and isolation of citrinalin and cyclopiamine congeners.

http://www.wikidata.org/entity/Q33980370

description

2014 nî lūn-bûn

@nan

2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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Total synthesis and isolation of citrinalin and cyclopiamine congeners.

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David E Williams

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Dean J Tantillo

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Eduardo V Mercado-Marin

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Eli F Pimenta

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Michael W Lodewyk

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Pablo Garcia-Reynaga

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Raymond J Andersen

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Richmond Sarpong

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Roberto G S Berlinck

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Stelamar Romminger

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P2860

Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids

Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids.

Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp

PF1270A, B and C, novel histamine H3 receptor ligands produced by Penicillium waksmanii PF1270.

Chemoselective and enantioselective oxidation of indoles employing aspartyl peptide catalysts.

Concise, stereocontrolled synthesis of the citrinadin B core architecture.

Enantioselective total synthesis of (-)-citrinadin A and revision of its stereochemical structure.

Naturally-occurring nitro compounds.

Computational prediction of 1H and 13C chemical shifts: a useful tool for natural product, mechanistic, and synthetic organic chemistry.

A general bifunctional catalyst for the anti-Markovnikov hydration of terminal alkynes to aldehydes gives enzyme-like rate and selectivity enhancements.

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Scott J. Miller

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