Journal ArticleDOI
A [W(CO)5·THF]-Mediated Pauson-Khand Reaction: Cyclizations of 1,6-Enynes via a Batch-Catalytic Protocol
Thomas R. Hoye,Joseph A. Suriano +1 more
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This article is published in Journal of the American Chemical Society.The article was published on 1993-02-01. It has received 74 citations till now. The article focuses on the topics: Pauson–Khand reaction & Enone.read more
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Recent Advances in the Pauson–Khand Reaction and Related [2+2+1] Cycloadditions
Kay M. Brummond,Joseph L. Kent +1 more
TL;DR: The Pauson-Khand reaction has been studied extensively in the literature as discussed by the authors, with a focus on cycloaddition precursors for natural product synthesis, such as dicobaltoctacarbonyl and traceless tethers.
Journal ArticleDOI
Molecular Design of Single-Site Metal Alkoxide Catalyst Precursors for Ring-Opening Polymerization Reactions Leading to Polyoxygenates. 1. Polylactide Formation by Achiral and Chiral Magnesium and Zinc Alkoxides, (η3-L)MOR, Where L = Trispyrazolyl- and Trisindazolylborate Ligands
Malcolm H. Chisholm,Nancy W. Eilerts,John C. Huffman,Suri S. Iyer,and Martha Pacold,Khamphee Phomphrai +5 more
TL;DR: In this paper, achiral and chiral C3-symmetric complexes LMOR have been synthesized and employed in the ring-opening polymerization of l-, rac-, and meso-lactide in CH2Cl2 at 25 °C and below.
Journal ArticleDOI
New Developments in the Pauson-Khand Reaction.
Oliver Geis,Hans-Günther Schmalz +1 more
TL;DR: Catalytic and asymmetric variations, enones, enynes, and allene as other starting materials, and numerous applications in natural product synthesis are all evidence of the diversity of the Pauson-Khand reaction, which now definitely counts among the standard tools of organic synthesis.