Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
about
1,7-octadiene-assisted tandem multicomponent cross-enyne metathesis (CEYM)-Diels-Alder reactions: a useful alternative to Mori's conditions.Synthesis of polycyclic benzofused nitrogen heterocycles via a tandem ynamide benzannulation/ring-closing metathesis strategy. Application in a formal total synthesis of (+)-FR900482Synthesis and biological evaluation of carbocyclic analogues of pachastrissamine.A one-pot, three-step process for the diastereoselective synthesis of aminobicyclo[4.3.0]nonanes using consecutive palladium(II)- and ruthenium(II)-catalysis.A metal-catalyzed enyne-cyclization step for the synthesis of bi- and tricyclic scaffolds amenable to molecular library production.Palladium-catalyzed 1,1-difunctionalization of ethylene.Ruthenium-catalyzed intramolecular [2+2+2] cycloaddition and tandem cross-metathesis of triynes and enediynes.(Hetero)aromatics from dienynes, enediynes and enyne-allenes.Recent advances in the Overman rearrangement: synthesis of natural products and valuable compounds.Biomimetic Assembly Lines Producing Natural Product Analogs: Strategies from a Versatile Manifold to Skeletally Diverse Scaffolds.Endo-selective enyne ring-closing metathesis promoted by stereogenic-at-Mo monoalkoxide and monoaryloxide complexes. Efficient synthesis of cyclic dienes not accessible through reactions with Ru carbenes.One-pot cross-enyne metathesis (CEYM)-Diels-Alder reaction of gem-difluoropropargylic alkynes.Ene-yne cross-metathesis with ruthenium carbene catalystsPropargyl vinyl ethers as heteroatom-tethered enyne surrogates: diversity-oriented strategies for heterocycle synthesis.Construction of the basic skeleton of ophiobolin A and variecolin.Excimer formation of 6-(1-pyrenyl)hexyl-11(1-pyrenyl)undecanoate within an ionic liquid and cosolvent-modified ionic liquid mixture.DFT study on the recovery of Hoveyda-grubbs-type catalyst precursors in enyne and diene ring-closing metathesis.Rh(I) -Catalyzed Cyclizative Addition Reaction of 1,6-Enyne and Sulfonyl Chloride by Carbophilic Activation.DFT study on the reaction mechanism of the ring closing enyne metathesis (RCEYM) catalyzed by molybdenum alkylidene complexes.Thiazolium salt-catalyzed C-C triple bond cleavage for accessing substituted 1-naphthols via benzannulation.Palladium-catalyzed oxidative 6-exo-trig cyclization of 1,6-enynes: facile synthesis of bicyclo[4.1.0]heptan-5-ones.Splitting a Substrate into Three Parts: Gold-Catalyzed Nitrogenation of Alkynes by C-C and C≡C Bond Cleavage.Diversity-oriented enantioselective synthesis of highly functionalized cyclic and bicyclic alcohols.Recent Progress on Enyne Metathesis: Its Application to Syntheses of Natural Products and Related Compounds.Synthetic approaches to selenacephams and selenacephems via a cleavage of diselenide and selenium anionDiscovery of a multi-bond forming, four-step tandem process: construction of drug-like polycyclic scaffoldsDomino ring-opening-ring-closing enyne metathesis vs enyne metathesis of norbornene derivatives with alkynyl side chains. Construction of condensed polycarbocycles
P2860
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P2860
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@ast
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@en
type
label
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@ast
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@en
prefLabel
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@ast
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@en
P2860
P356
P1476
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles.
@en
P2093
Hélène Villar
P2860
P356
10.1039/B508899M
P577
2006-10-04T00:00:00Z