A Mechanistic Dichotomy in Ruthenium-Catalyzed Propargyl Alcohol Reactivity: A Novel Hydrative Diyne Cyclization
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja036410f
Reference7 articles.
1. An Unusual Ruthenium-Catalyzed Cycloisomerization of Alkynes and Propargyl Alcohols
2. Selective Linear Coupling Reaction of Acetylene and Acrylonitrile Catalyzed by the Well-Defined Metallacyclopentadiene Complex C5Me5(PPh3)(Cl)RuCHCHCHCH
3. An Unusual Ruthenium-Catalyzed Dimerization of Propargyl Alcohols
4. Ruthenium-Catalyzed Alkyne−Propargyl Alcohol Addition. An Asymmetric Total Synthesis of (+)-α-Kainic Acid
5. [RuCp(PR3)(CH3CN)2]PF6 (R = Ph, Me, Cy). Convenient Precursors for Mixed Ruthenium(II) and Ruthenium(IV) Half-Sandwich Complexes
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