Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
about
Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.An expeditious total synthesis of both diastereoisomeric lipid dihydroxytetrahydrofurans from Notheia anomala.Stereochemistry of ring-opening/cross metathesis reactions of exo- and endo-7-oxabicyclo[2.2.1]hept-5-ene-2-carbonitriles with allyl alcohol and allyl acetateManipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperatureSynthesis of Aromatic Retinoids and Curcuminoids and Evaluation of their Antiproliferative, Antiradical, and Anti-inflammatory ActivitiesA phosphate tether-mediated, one-pot, sequential ring-closing metathesis/cross-metathesis/chemoselective hydrogenation protocolGrubbs cross-metathesis pathway for a scalable synthesis of γ-keto-α,β-unsaturated esters.Glycosyl-Templated Chiral Helix Stapling of Ethynylpyridine Oligomers by Alkene Metathesis between Inter-Pitch Side Chains.Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes.Divergent pathways and competitive mechanisms of metathesis reactions between 3-arylprop-2-ynyl esters and aldehydes: an experimental and theoretical study.Isovanillin derived N-(un)substituted hydroxylamines possessing an ortho-allylic group: valuable precursors to bioactive N-heterocycles.Asymmetric Synthesis of Pyrrolidine-Containing Chemical Scaffolds via Tsuji-Trost Allylation of N-tert-Butanesulfinyl Imines.Design, Synthesis, and Self-Assembly Behavior of Liquid-Crystalline Bis-[60]Fullerodendrimers.Diastereoselective synthesis of novel heterocyclic scaffolds through tandem Petasis 3-component/intramolecular Diels-Alder and ROM-RCM reactions.Design and Stereoselective Synthesis of ProM-2: A Spirocyclic Diproline Mimetic with Polyproline Type II (PPII) Helix Conformation.Reactivity in organised assembliesCarbonylative coupling of allylic acetates with aryl boronic acids
P2860
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P2860
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@en
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@nl
type
label
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@en
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@nl
prefLabel
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@en
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@nl
P2093
P2860
P356
P1476
Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.
@en
P2093
Bruce H Lipshutz
Karl Voigtritter
Subir Ghorai
P2860
P304
P356
10.1021/JO200360S
P407
P577
2011-04-29T00:00:00Z