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Journal ArticleDOI

Preparations of bicycliclactols from allyl and/or homoallyl propargyl acetal-cobalt complexes and its application to the formal synthesis of (±) loganine

TLDR
In this article, the corresponding bis(allyl or homoallyl)propargyl acetal-cobalt complexes in the presence of trimethylamine Noxide were used for the formal synthesis of loganine.
About
This article is published in Tetrahedron Letters.The article was published on 1993-06-18. It has received 42 citations till now. The article focuses on the topics: Propargyl & Enone.

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Recent Advances in the Pauson–Khand Reaction and Related [2+2+1] Cycloadditions

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

Pauson−Khand Reactions of Electron‐Deficient Alkenes

TL;DR: Despite the common perception that alkenes possessing electron-withdrawing groups are not adequate substrates for Pauson−Khand (PK) reactions, a number of successful examples of this reaction involving electron-deficient alkenses, such as α,β-unsaturated ketones, esters, nitriles, sulfoxides and sulfones, have been reported in recent years as discussed by the authors.
References
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Book

The Total Synthesis of Natural Products

John ApSimon
TL;DR: The Total Synthesis of Macrocyclic Lactones Synthesis for the Leukotrienes Synthesis as discussed by the authors, 1980 - 1986, is a classic work in the field of macrocyclic lactones.
Journal ArticleDOI

Preparation and use of tetra-n-butylammonium per-ruthenate (TBAP reagent) and tetra-n-propylammonium per-ruthenate (TPAP reagent) as new catalytic oxidants for alcohols

TL;DR: Tetra-n-butylammonium per-ruthenate (Bun4N)(RuO4) and tetra n-propylammonmonium (Prn4N), with N-methylmorpholine N-oxide, function as mild catalytic oxidants for the high yield conversion of alcohols to aldehydes and ketones and are competitive with more conventional reagents as mentioned in this paper.
Journal ArticleDOI

N-oxide promoted pauson-khand cyclizations at room temperature

TL;DR: Tertiary amine oxides have been utilized to effect cobalt-mediated intramolecular cyclizations of enynes (Pauson-Khand reactions) at room temperature as discussed by the authors.
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