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Journal ArticleDOI

tert-Butyldimethylsilyldihalomethyllithium as a dihalomethylene dianion synthon. 1,3-Rearrangement and 1,4-rearrangement of silyl group from carbon to oxide

TLDR
One-pot synthesis of R 1 CH(OSiMe 2 - t -Bu)CX 2 CH(OH)R 2 (X=Cl, Br) successive addition of two different aldehydes (R 1 CHO and R 2 CHO) has been achieved starting from tert -butyldimethylsilyldihalomethyllithium as mentioned in this paper.
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This article is published in Tetrahedron.The article was published on 1996-01-08. It has received 58 citations till now. The article focuses on the topics: Carbanion & Ether.

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Citations
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Natural product synthesis using multicomponent reaction strategies.

TL;DR: The preparation of urea by Wöhler constituted a landmark achievement in organic chemistry, and it laid the ground for the early days of target-oriented organic synthesis, a task deemed inconceivable by early practitioners.
Journal ArticleDOI

Small Heterocycles in Multicomponent Reactions

TL;DR: This paper presents a meta-analyses of the proton-probes of Na6(SO4)2, Na4, and Na4 of the nucleus of the H2O2 molecule and shows clear patterns in the response of these two mechanisms to each other.
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The role of 1,3-dithianes in natural product synthesis

TL;DR: Foubelo et al. as mentioned in this paper studied carbanions, organolithium compounds, and dithioacetal moiety in the tetrahedron of the Tetrarch.
References
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Triethylborane-Induced Hydrodehalogenation of Organic Halides by Tin Hydrides

TL;DR: The reduction of organic halides with tributyltin hydride in the presence of a catalytic amount of triethylborane has been studied in this paper, and the reduction of alkenyl halides and alkyl bromides with n-Bu3SnH-Et3B system was not so effective.
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Umsetzung metallierter Trimethylsilylformaldehyd-thioacetale mit Carbonylverbindungen. Eine einfache Methode großer Anwendungsbreite zur Herstellung von Keten-thioacetalen

TL;DR: In this paper, a simple method of broad applicability for the preparation of ketene thioacetals was proposed for the Preparation of Ketene Thioacetal (KTE) compounds.
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