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Journal ArticleDOI

Concise, Stereoselective Approach to the Spirooxindole Ring System of Citrinadin A

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TLDR
The spirooxindole ring system of citrinadin A has been synthesized with excellent control over the absolute stereochemistry at the spirocenter using a novel diastereoselective DMDO-mediated oxidative rearrangement employing an 8-phenylmenthol chiral auxiliary on the indole nitrogen.
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This article is published in Organic Letters.The article was published on 2007-10-06. It has received 66 citations till now. The article focuses on the topics: Ring (chemistry).

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Highly Enantioselective [3+2] Annulation of Morita–Baylis–Hillman Adducts Mediated by L‐Threonine‐Derived Phosphines: Synthesis of 3‐Spirocyclopentene‐2‐oxindoles having Two Contiguous Quaternary Centers

TL;DR: The Morita-Baylis-Hillman (MBH) carbonates (II, (IV), and (VII) serve as C3 synthons in asymmetric [3 + 2] annulation reactions to give a series of 3-spirocyclopentene-2-oxindoles with two contiguous quaternary centers such as (III, (V), or (VIII) as present in various alkaloids as discussed by the authors.
Journal ArticleDOI

Molecular diversity of spirooxindoles. Synthesis and biological activity

TL;DR: This review focuses on the various strategies for the enantioselective synthesis of spirocyclic oxindoles relying on reports over the past decade and from earlier work.
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Palladium‐Catalyzed Tandem Heck Reaction/C ? H Functionalization—Preparation of Spiro‐Indane‐Oxindoles

TL;DR: An efficient preparation of spiro-fused indane-oxindoles by carbopalladation to form an alkylpalladium intermediate and subsequent functionalization of an unactivated aryl C H bond is reported.
Journal ArticleDOI

Methods for direct alkene diamination, new & old

TL;DR: The purpose of this review is to provide an overview of all methods of direct alkene diamination, metal-mediated or otherwise.
References
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Journal ArticleDOI

Marine-derived fungi: a chemically and biologically diverse group of microorganisms

TL;DR: A diverse array of secondary metabolites have been isolated and characterized from marine-derived fungi and the structures and biological activities of these metabolites are presented.
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Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines

TL;DR: Davis as discussed by the authors was a pioneer in asymmetric synthesis, and developed a new method for stereoselective fluorination of organic molecules, which is a recent focus of his research at Drexel University.
Journal ArticleDOI

An Efficient Catalytic Asymmetric Epoxidation Method

TL;DR: In this paper, a catalytic asymmetric epoxidation method for olefins using potassium peroxomonosulfate (Oxone, Dupont) as oxidant and a fructose-derived ketone (1) as catalyst is described.
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