Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction.
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Bioinspired iterative synthesis of polyketidesA ligand-directed divergent catalytic approach to establish structural and functional scaffold diversity.Chemoselective oxidation of aryl organoboron systems enabled by boronic acid-selective phase transferAssembly-line synthesis of organic molecules with tailored shapesRu-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studiesProtecting group-free, selective cross-coupling of alkyltrifluoroborates with borylated aryl bromides via photoredox/nickel dual catalysis.From synthesis to function via iterative assembly of N-methyliminodiacetic acid boronate building blocks.MIDA boronates are hydrolysed fast and slow by two different mechanisms.Lessons from the synthetic chemist nature.Linchpin dienes: key building-blocks in the synthesis of polyenic frameworks.Sequential and iterative Pd-catalyzed cross-coupling reactions in organic synthesis.Recent Advances in Boron-Substituted 1,3-Dienes Chemistry: Synthesis and Application.Iterative protecting group-free cross-coupling leading to chiral multiply arylated structures.Short Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line Synthesis.Chemoselective boronic ester synthesis by controlled speciation.Syntheses of Denudatine Diterpenoid Alkaloids: Cochlearenine, N-Ethyl-1α-hydroxy-17-veratroyldictyzine, and Paniculamine.Synthesis of many different types of organic small molecules using one automated process.A General Protocol for the Polycondensation of Thienyl N-Methyliminodiacetic Acid Boronate Esters To Form High Molecular Weight Copolymers.Synthetic fermentation of bioactive non-ribosomal peptides without organisms, enzymes or reagents.C(sp3)-C(sp2) cross-coupling of alkylsilicates with borylated aryl bromides - an iterative platform to alkylated aryl- and heteroaryl boronatesUse of N-methyliminodiacetic acid boronate esters in suzuki-miyaura cross-coupling polymerizations of triarylamine and fluorene monomers.Facile synthesis of borofragments and their evaluation in activity-based protein profiling.The natural productome.Iterative reactions of transient boronic acids enable sequential C-C bond formation.Chemoselective Suzuki-Miyaura Cross-Coupling via Kinetic Transmetallation.Amphoteric Borylketenimines: Versatile Intermediates in the Synthesis of Borylated Heterocycles.Stereoselective Direct Chlorination of Alkenyl MIDA Boronates: Divergent Synthesis of E and Z α-Chloroalkenyl Boronates.Zeolite-Based Organic Synthesis (ZeoBOS) of Acortatarin A: First Total Synthesis Based on Native and Metal-Doped Zeolite-Catalyzed Steps.Dehydrogenative desaturation-relay via formation of multicenter-stabilized radical intermediates.Palladium-catalysed atom-economical synthesis of conjugated dienals from terminal acetylenes and acrolein.The Molecular Industrial Revolution: Automated Synthesis of Small Molecules.Tandem Chemoselective Suzuki-Miyaura Cross-Coupling Enabled by Nucleophile Speciation Control.Direct catalytic cross-coupling of alkenyllithium compounds.Toward Generalization of Iterative Small Molecule SynthesisMicrowave (MW), Ultrasound (US) and Combined Synergic MW-US Strategies for Rapid Functionalization of Pharmaceutical Use Phenols
P2860
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P2860
Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction.
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
Synthesis of most polyene natu ...... cks and one coupling reaction.
@en
type
label
Synthesis of most polyene natu ...... cks and one coupling reaction.
@en
prefLabel
Synthesis of most polyene natu ...... cks and one coupling reaction.
@en
P2093
P2860
P356
P1433
P1476
Synthesis of most polyene natu ...... cks and one coupling reaction.
@en
P2093
Eric M Woerly
Jahnabi Roy
Martin D Burke
P2860
P2888
P304
P356
10.1038/NCHEM.1947
P577
2014-06-01T00:00:00Z
P6179
1020633119