Protecting-group-free synthesis as an opportunity for invention.
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Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon11-Step Total Synthesis of Pallambins C and DPhotochemical Approaches to Complex Chemotypes: Applications in Natural Product SynthesisThe economies of synthesis.Boron-based dipolar multicomponent reactions: simple generation of substituted aziridines, oxazolidines and pyrrolidines.Chemo- and site-selective derivatizations of natural products enabling biological studies.Marine Rare Actinobacteria: Isolation, Characterization, and Strategies for Harnessing Bioactive Compounds.Self-sorting of dynamic imine libraries during distillation.Enantioselective synthesis of tatanans A-C and reinvestigation of their glucokinase-activating properties.An efficient, modular approach for the synthesis of (+)-strictifolione and a related natural product.Creation of an α-mannosynthase from a broad glycosidase scaffold.A modular phosphate tether-mediated divergent strategy to complex polyols.A Reactivity-Driven Approach to the Discovery and Development of Gold-Catalyzed Organic Reactions.Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.Exploration of cascade cyclizations terminated by tandem aromatic substitution: total synthesis of (+)-schweinfurthin A.Total (bio)synthesis: strategies of nature and of chemists.A one-pot multicomponent coupling/cyclization for natural product herbicide (±)-thaxtomin A.Nature-inspired total synthesis of (-)-fusarisetin A.Site-Selective Acylations with Tailor-Made Catalysts.A concise asymmetric total synthesis of (+)-brevisamide.Native serotonin membrane receptors recognize 5-hydroxytryptophan-functionalized substrates: enabling small-molecule recognition.Enhanced site-selectivity in acylation reactions with substrate-optimized catalysts on solid supports.Fusarisetin A: Scalable Total Synthesis and Related Studies.Aqueous Glycosylation of Unprotected Sucrose Employing Glycosyl Fluorides in the Presence of Calcium Ion and Trimethylamine.Practical carbon-carbon bond formation from olefins through nickel-catalyzed reductive olefin hydrocarbonation.Phosphate-tether-mediated ring-closing metathesis for the preparation of complex 1,3-anti-diol-containing subunits.A phosphate tether-mediated, one-pot, sequential ring-closing metathesis/cross-metathesis/chemoselective hydrogenation protocolChemoselectivity and the curious reactivity preferences of functional groups.Hypervalent iodine reagents in the total synthesis of natural products.Chemical synthesis of the englerins.Lead-oriented synthesis: a new opportunity for synthetic chemistry.Is there no end to the total syntheses of strychnine? Lessons learned in strategy and tactics in total synthesisChemoselective hydroxyl group transformation: an elusive target.Strained cyclophane natural products: macrocyclization at its limits.Catalytic selective synthesis.Natural product synthesis in the age of scalability.Azabicycles construction: the transannular ring contraction with N-protected nucleophiles.Orthogonality in organic, polymer, and supramolecular chemistry: from Merrifield to click chemistry.Enantioselective total syntheses of (-)-palau'amine, (-)-axinellamines, and (-)-massadines.Asymmetric Iridium-Catalyzed C-C Coupling of Chiral Diols via Site-Selective Redox-Triggered Carbonyl Addition
P2860
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P2860
Protecting-group-free synthesis as an opportunity for invention.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Protecting-group-free synthesis as an opportunity for invention.
@en
Protecting-group-free synthesis as an opportunity for invention.
@nl
type
label
Protecting-group-free synthesis as an opportunity for invention.
@en
Protecting-group-free synthesis as an opportunity for invention.
@nl
prefLabel
Protecting-group-free synthesis as an opportunity for invention.
@en
Protecting-group-free synthesis as an opportunity for invention.
@nl
P356
P1433
P1476
Protecting-group-free synthesis as an opportunity for invention.
@en
P2093
Ian S Young
Phil S Baran
P2888
P304
P356
10.1038/NCHEM.216
P577
2009-06-01T00:00:00Z