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Journal ArticleDOI

A Versatile and Efficient Synthesis of Annulated Cyclopentanes by Stereoselective [3 + 2] Cycloaddition of Allylsilanes and Cycloalkenyl Methyl Ketones

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This article is published in Angewandte Chemie.The article was published on 1993-07-01. It has received 65 citations till now. The article focuses on the topics: Cyclopentanes & Enone.

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Allylsilanes in Organic Synthesis − Recent Developments

TL;DR: A survey of the most recent advances in this field is described in this paper, including transformations of allylsilanes through electrophilic, radical and organometallic processes, with particular emphasis on the stereocontrol arising from these processes.
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New Developments in the Cyclopentadienyl Chemistry of the Alkaline-Earth Metals

TL;DR: Recent developments in the chemistry of cyclopentadienyl derivatives of the alkaline-earth (group 2) metals are reviewed in this paper, where new complexes and their applications in organometallic and materials synthesis reflect the growing number of ways that can be used to manipulate the alkalinear-earth−cyclopentadiyl bond.
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Catalytic Asymmetric [3+2] Annulation of Allylsilanes with Isatins: Synthesis of Spirooxindoles

TL;DR: In the presence of chiral ScCl2(SbF6)·BIOP, prepared in situ, and TmsCl as an essential promoter, the desired spirooxindoles are obtained with excellent enantioselectivities at room temperature as mentioned in this paper.
References
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Journal ArticleDOI

The interaction of silicon with positively charged carbon

TL;DR: Sommer et al. as mentioned in this paper showed that a silyl group beta to the leaving group enormously enhances the rate of solvolysis, and that a gamma silyal group also has an enhancing effect, but that an alpha sily l group actually decreases reactivity in comparison with hydrocarbon models.
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Kinetics of the reactions of allylsilanes, allylgermanes, and allylstannanes with carbenium ions

TL;DR: In this article, the second-order rate constants for the reactions of para-substituted diarylmrbenium ions with allylsilanes 2, allylgermanes 3, and allylstannanes 4 have been determined in CH2C12 solution at -70 to -30 OC.
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